Transpac™/Transtar™

TRANSPAC™ / TRANSTAR™ 15' BIFURCATED CABLE FOR USE WITH DISPOSABLE TRANSDUCER REUSABLE: Do Not Discard

Registry build 21.09.26
7manufacturers in China registered for this device type
58catalogue numbers in this listing
40recalls on this code

Who Else Makes It

Concentrated in Guangdong (5), Zhejiang (1), Shandong (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DRS
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Bioxin Medical Co., Ltd. Weihai Shandong Contract manufacturer 8
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
Orantech Inc. Shenzhen Guangdong Contract manufacturer 40
Zhejiang Haisheng Medical Device Co., Ltd. Shaoxing Zhejiang Contract manufacturer 21
Unimed Medical Supplies Inc Shenzhen Guangdong Contract manufacturer 15
Shenzhen Antmed Co., Ltd. Dongguan Guangdong Manufacturer 4

Record

Regulatory record for Transpac™/Transtar™
Listed by ICU Medical, Inc, United States
FDA product code DRS
Device type Transducer, Blood-Pressure, Extravascular
Device class Class 2
Regulation 21 CFR 870.2850
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K061573
Record published 2024-08-20

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Transpac™/Transtar™
Catalogue number Size Status
42661-62 In distribution
886-42661-27 In distribution
42773-05 In distribution
427720448 In distribution
42667-14 In distribution
42671-14 In distribution
42671-27 In distribution
42773-43 In distribution
42667-27 In distribution
42661-69 In distribution
42773-21 In distribution
42661-30 In distribution
42661-04 In distribution
42773-22 In distribution
42773-14 In distribution
42661-74 In distribution
42661-03 In distribution
42773-27 In distribution
42661-22 In distribution
427720440 In distribution
42661-14 In distribution
42772-04 In distribution
426610440 In distribution
011-42661-64 In distribution
011-42773-14 In distribution
42661-48 In distribution
42661-41 In distribution
42661-36 In distribution
42667-36 In distribution
42773-36 In distribution
42772-36 In distribution
011-42669-73 In distribution
1042661061027 In distribution
42661-66 In distribution
42661-70 In distribution
42772-27 In distribution
42773-04 In distribution
011-42773-27 In distribution
426610439 In distribution
42775-27 In distribution
42661-57 In distribution
427730447 In distribution
42661-68 In distribution
42661-24 In distribution
42671-36 In distribution
42661-21 In distribution
42772-22 In distribution
42772-14 In distribution
42661-35 In distribution
42773-40 In distribution
42661-61 In distribution
42661-43 In distribution
42661-05 In distribution
42661-27 In distribution
42661-45 In distribution
42772-05 In distribution
42661-42 In distribution
011-42775-27 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ICU Medical ICU Medical, Inc 381
Medex ICU Medical, Inc 225
Biotrans™ Pressure Monitoring Kits Bioptimal International Pte. Ltd. 134
Transpac™ ICU Medical, Inc 117
Antmed Shenzhen Antmed Co., Ltd. 96
Namic Navilyst Medical, Inc. 60
Namic Medline Industries, Inc. 58
Merit Medical® Argon Critical Care Systems Singapore PTE. Ltd. 28
Centurion Centurion Medical Products Corporation 23
Transducer, Blood-Pressure, Extravascular Utah Medical Products, Inc. 22
Deltran Utah Medical Products, Inc. 22
Unimed Unimed Medical Supplies Inc 17

Showing 12 of 145. All products under Transducer, Blood-Pressure, Extravascular

Recalls Naming This Product

193 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Transpac™/Transtar™
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 20 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
60,560 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
130 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
140 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
260 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
380 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
340 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
260 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
3060 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
4580 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
2310 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
520 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
3640 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
38160 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
3480 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
17420 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
800 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
4360 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
1740 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
500 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
4470 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits
containing the Transpac IV transducers.
730 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 40 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 40 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 200 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 3460 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 2240 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 900 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 3020 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 11100 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 2900 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 280 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 820 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 1960 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 200 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 2200 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 60 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 1100 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 740 units 2017-07-11
ICU Medical, Inc 510(k) number 2016-09-27 Class II Device Design ICU Medical Inc. has identified a potential for leak with certain SafeSet Reservoir and blood sampling kits containing the Transpac IV transducers. 710 units 2017-07-11

Showing 40 of 193.

Recalls

12 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2023-11-10 Class II Nonconforming Material/Component There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inadequate seal may lead to a leak during infusion of medication 31,685 total
2023-11-10 Class II Nonconforming Material/Component There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inadequate seal may lead to a leak during infusion of medication 31,685 total
2023-11-10 Class II Nonconforming Material/Component There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inadequate seal may lead to a leak during infusion of medication 31,685 total
2023-11-10 Class II Nonconforming Material/Component There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inadequate seal may lead to a leak during infusion of medication 31,685 total
2023-11-10 Class II Nonconforming Material/Component There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inadequate seal may lead to a leak during infusion of medication 31,685 total
2023-11-10 Class II Nonconforming Material/Component There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inadequate seal may lead to a leak during infusion of medication 31,685 total
2023-11-10 Class II Nonconforming Material/Component There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inadequate seal may lead to a leak during infusion of medication 31,685 total
2023-11-10 Class II Nonconforming Material/Component There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inadequate seal may lead to a leak during infusion of medication 31,685 total
2023-11-10 Class II Nonconforming Material/Component There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inadequate seal may lead to a leak during infusion of medication 31,685 total
2018-11-27 Class II Process design Reports of pressure tubing separation between the sampling port and the high pressure tubing on certain lots of extravascular blood pressure transducers, which could lead to delay in therapy, and in rare circumstances, pressure tubing separ 5000 2022-02-01
2018-11-27 Class II Process design Reports of pressure tubing separation between the sampling port and the high pressure tubing on certain lots of extravascular blood pressure transducers, which could lead to delay in therapy, and in rare circumstances, pressure tubing separ 2022-02-01
2018-11-27 Class II Process design Reports of pressure tubing separation between the sampling port and the high pressure tubing on certain lots of extravascular blood pressure transducers, which could lead to delay in therapy, and in rare circumstances, pressure tubing separ 280 2022-02-01

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer