Truwave, Vamp

45 catalogue numbers from PXVK0481, listed by Edwards Lifesciences Technology Sarl, United States, under Transducer, Pressure, Catheter Tip. 4 manufacturers in China are registered for this product code.

Registry build 21.09.26
4manufacturers in China registered for this device type
45catalogue numbers in this listing
5510(k) clearances naming this product code
10recalls on this code

Who Else Makes It

Concentrated in Shanghai (1), Guangdong (1), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code DXO
Manufacturer City Province Registered as Device types
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Suzhou Prosteri Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 20
Beijing Bywave Sensing Medical Technology Co., Ltd. Beijing Beijing Manufacturer 2

Record

Regulatory record for Truwave, Vamp
Listed by Edwards Lifesciences Technology Sarl, United States
FDA product code DXO
Device type Transducer, Pressure, Catheter Tip
Device class Class 2
Regulation 21 CFR 870.2870
Establishment Contract manufacturer, Specification developer, Manufacturer
510(k) K142749
Record published 2016-09-03
Record revised 2024-02-28 (version 7)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: STORE IN A COOL, DRY PLACE.
Packaging Shipper of 10, shipper of 20, shipper of 5, case of 10, case of 20, case of 8
Sizes Total volume 3 ml; length 235 cm

Catalogue Numbers

Catalogue numbers for Truwave, Vamp
Catalogue number Size Status
PXVK0481 Total Volume 3 ml In distribution
T005050M Volume 3 cc Length 235 cm In distribution
PXVK0755 Total Volume 3 ml In distribution
PXVMP2X31 Total Volume 3 ml In distribution
PXVK0437 Total Volume 3 ml In distribution
PXVK0797 Total Volume 3 ml In distribution
T005048B TOTAL VOLUME: 3 CC, LENGTH: 78 INCH (200 CENTIMETER) In distribution
T001745A TOTAL VOLUME: 3 CC, LENGTH: 72 INCH (180 CENTIMETER) In distribution
PXVK0789 TOTAL VOLUME: 3 MILLILITER, LENGTH: 84 INCH (210 CENTIMETER) In distribution
PXVK1079 Total Volume 3 ml In distribution
PXVK1041 Total Volume 3 ml In distribution
T100500A Total Volume 3 ml In distribution
PXVK1076 Total Volume 3 ml In distribution
T310845A Total Volume: 30cc, Length 67 Inch (171 Centimeter) In distribution
PXVK0363 Total Volume 3 ml In distribution
PXVMP260 TOTAL VOLUME: 3 CC, LENGTH: 60 INCH (150 CENTIMETER) In distribution
PXVK0738 Total Volume 3 ml In distribution
PXVMP3X31 Total Volume 3 ml In distribution
PXVMP2X21 Total Volume 3 ml In distribution
T001741A TOTAL VOLUME: 3 CC, LENGTH: 72 INCH (180 CENTIMETER) In distribution
PXVK1102 TOTAL VOLUME: 3 MILLILITER, LENGTH: 52 INCH (132 CENTIMETER) In distribution
PXVK0398 Total Volume 3 ml In distribution
PXVK0994 Total Volume 3 ml In distribution
PXVK0996 TOTAL VOLUME: 3 CC, LENGTH: 68 INCH (174 CENTIMETER) In distribution
PXVK0670 TOTAL VOLUME: 3 CC, LENGTH: 75 INCH (190 CENTIMETER) In distribution
PXVK0965 Total Volume 3 ml In distribution
PXVK1099 TOTAL VOLUME: 3 MILLILITER, LENGTH: 62 INCH (157 CENTIMETER) In distribution
PXVK0412 TOTAL VOLUME: 3 CC, LENGTH: 78 INCH (198 CENTIMETER) In distribution
T431305A TOTAL VOLUME: 3 MILLILITER, LENGTH: 75 INCH (190 CENTIMETER) In distribution
PXVMP184 TOTAL VOLUME: 3 CC, LENGTH: 84 INCH (210 CENTIMETER) In distribution
T490009M In distribution
PXVK1086 Total Volume 3 ml In distribution
T433806A TOTAL VOLUME: 3 CC, LENGTH: 87 INCH (220 CENTIMETER) In distribution
PXVK1075 TOTAL VOLUME: 3 MILLILITER, LENGTH: 76 INCH (193 CENTIMETER) In distribution
PXVK1003 Total Volume 3 ml In distribution
PXVK275 Total Volume 3 ml In distribution
T001737A TOTAL VOLUME: 3 CC, LENGTH: 72 INCH (180 CENTIMETER) In distribution
PXVK093 TOTAL VOLUME: 3 CC, LENGTH: 81 INCH (206 CENTIMETER) In distribution
PXVK268 Total Volume 3 ml In distribution
PXVK220 Total Volume 3 ml In distribution
T001744M Length 235.0000 cm In distribution
PXVK0478 Total Volume 3 ml In distribution
PXVK282 Total Volume 3 ml In distribution
PXVK0802 TOTAL VOLUME: 3 CC, LENGTH: 84 INCH (213 CENTIMETER) In distribution
PXVMP272 TOTAL VOLUME: 3 CC, LENGTH: 72 INCH (180 CENTIMETER) In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Truwave Edwards Lifesciences Technology Sarl 456
OptoMonitor 3 Opsens Inc. 73
Truwave, Vamp Plus Edwards Lifesciences Technology Sarl 24
PX1800 → Truwave Cables Edwards Lifesciences Technology Sarl 22
Truwave, Vamp JR Edwards Lifesciences Technology Sarl 12
Truwave Cables Edwards Lifesciences Technology Sarl 7
TruWave, Vamp Plus Becton, Dickinson AND Company 5
TruWave Becton, Dickinson AND Company 4
Comet Boston Scientific Corporation 4
Medline Industries, Inc. Medline Industries, Inc. 4
Pressure Tubing Edwards Lifesciences Technology Sarl 3
OptoMonitor Opsens Inc. 3

Showing 12 of 63. All products under Transducer, Pressure, Catheter Tip

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K222216 2022-12-22
K171996 2017-10-23
K142749 2015-01-18
K141495 2014-09-03
K053016 2005-12-30

Recalls Naming This Product

12 recalls name this product by its own identifiers, the UDI on its label or the 510(k) it is cleared under.

Recalls naming the identifiers of Truwave, Vamp
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Edwards Lifesciences Technology Sarl UDI-DI 2023-10-04 Class II Device Design Their is the potential for flushing difficulties during setup of the pressure monitoring kit with pressure transducer. 118,570 units
Edwards Lifesciences Technology Sarl UDI-DI 2023-10-04 Class II Device Design Their is the potential for flushing difficulties during setup of the pressure monitoring kit with pressure transducer. 168,014 units
Edwards Lifesciences Technology Sarl 510(k) number 2021-05-26 Class II Under Investigation by firm There is a potential that the pressure tubing may detach from the blood sampling system 460 units 2023-12-14
Edwards Lifesciences Technology Sarl 510(k) number 2021-05-26 Class II Under Investigation by firm There is a potential that the pressure tubing may detach from the blood sampling system 700 units 2023-12-14
Edwards Lifesciences Technology Sarl 510(k) number 2021-05-26 Class II Under Investigation by firm There is a potential that the pressure tubing may detach from the blood sampling system 290 units 2023-12-14
Edwards Lifesciences Technology Sarl 510(k) number 2021-05-26 Class II Under Investigation by firm There is a potential that the pressure tubing may detach from the blood sampling system 2,000 units 2023-12-14
Edwards Lifesciences Technology Sarl 510(k) number 2021-05-26 Class II Under Investigation by firm There is a potential that the pressure tubing may detach from the blood sampling system 1,679 units 2023-12-14
Edwards Lifesciences Technology Sarl 510(k) number 2021-05-26 Class II Under Investigation by firm There is a potential that the pressure tubing may detach from the blood sampling system 990 units 2023-12-14
Edwards Lifesciences Technology Sarl 510(k) number 2021-05-26 Class II Under Investigation by firm There is a potential that the pressure tubing may detach from the blood sampling system 50 units 2023-12-14
Edwards Lifesciences Technology Sarl 510(k) number 2021-05-26 Class II Under Investigation by firm There is a potential that the pressure tubing may detach from the blood sampling system 90 units 2023-12-14
Edwards Lifesciences Technology Sarl 510(k) number 2015-07-31 Class II Device Design Flow restriction issues in a trifurcated IV set included in the pressure transducer kits. A restriction of the flow of IV fluid would result in either an inability to prime the system before use or difficulty in flushing the line after a bl 13,077 (U.S.) and 12,306 (International) 2016-07-08
Edwards Lifesciences Technology Sarl 510(k) number 2013-01-30 Class II Process change control The device is being recalled because the firm has received multiple complaints related to incorrect assembly that may result in dilution of blood samples. 30,467 2016-03-10

Recalls

1 of these is 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
2015-11-13 Class II Under Investigation by firm Edward Lifesciences is recalling Intravascular (IV)
Administration Sets due to the requirement of an additional FDA submission to support commercialization (clearance) of the devices.
147,350 units 2016-07-15

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