Transducer Cover

Sterile (3.5 x 20cm) latex cover for use with BK Medical 5P1, 8538, 8545, 8547, 8551, 8553, 8556, 8557, 8559, 8645, 8656, 8657, 8659, 8667, 8803, 8837, 8838 and E14C4 transducers

Registry build 21.09.26
44manufacturers in China registered for this device type
54catalogue numbers in this listing
15510(k) clearances naming this product code
28recalls on this code

Who Else Makes It

Concentrated in Guangdong (18), Jiangsu (10), Shanghai (3). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code ITX
Manufacturer City Province Registered as Device types
Jabil Circuit (Shanghai) Ltd. Shanghai Shanghai Contract manufacturer 31
Ming FAI Industrial (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 17
ATL Technology DG,Ltd. Dongguan Guangdong Contract manufacturer 14
Xuzhou Yongkang Electronic Science Technology Co., Ltd. Xuzhou Jiangsu Contract manufacturer 13
Hony Medical Co., Ltd. Taishan Guangdong Contract manufacturer 10
Xian Friendship Medical Electronics Co., Ltd. Xi’An Shaanxi Contract manufacturer 10
Taijia Medical Electronics (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 10
Chison Medical Technologies Co., Ltd. Wuxi Jiangsu Contract manufacturer 5
Philips Ultrasound (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 5
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56

Showing 12 of 44. All 44 manufacturers in China registered for Transducer, Ultrasonic, Diagnostic

Record

Regulatory record for Transducer Cover
Listed by Civco Medical Instruments Co., Inc., United States
FDA product code ITX
Device type Transducer, Ultrasonic, Diagnostic
Device class Class 2
Regulation 21 CFR 892.1570
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K970513
Record published 2021-12-07
Record revised 2022-03-22 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Ethylene Oxide
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Latex Contains natural rubber latex
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: Keep Away from Sunlight
Packaging Pack of 24, pack of 200, pack of 250, pack of 5, pack of 10
Sizes Width 1.3 to 17.8 cm; length 5.8 to 147 cm; width 0.94 to 96 in; length 2.6 to 33 in
Distribution end date 2022-09-30

Catalogue Numbers

Catalogue numbers for Transducer Cover
Catalogue number Size Per pack Status
610-2424 200 In distribution
610-2423 10 In distribution
610-985 Width 1.26 in In distribution
610-1271 Width 14 cm In distribution
610-1269 Length 61 cm In distribution
610-011 Width 1.38 in 24 In distribution
610-249 Length 20 cm 100 In distribution
610-015 Width 4 in In distribution
H2O-024 50 In distribution
610-020 Length 24 in In distribution
H2O-016TR In distribution
610-043 Length 30 cm In distribution
H2O-009TR In distribution
8990426 Width 1.3 in In distribution
610-208 Width 6 in In distribution
UA0006 Length 20 cm In distribution
610-044 Length 45 cm In distribution
610-2462 In distribution
610-046 Width 10 cm In distribution
H2O-023 50 In distribution
8990418 Width 1.3 in 100 In distribution
610-022 Width 9 in In distribution
610-2313 In distribution
610-013 Width 2 in In distribution
H2O-018TR In distribution
610-262 Length 20 cm 500 In distribution
H2O-022 50 In distribution
UA0032 Length 32 cm 24 In distribution
H2O-021 50 In distribution
H2O-020TR In distribution
UA0069 Length 32 cm In distribution
610-010 Width 1.4 in 50 In distribution
610-2425 200 In distribution
610-795 Length 12.8 in 24 In distribution
610-1303 Length 61 cm In distribution
610-2328, 610-2328-5 Width 96 in In distribution
610-2396 200 In distribution
610-1272 Length 91.5 cm In distribution
610-1270 Width 14 cm In distribution
H2O-005TR In distribution
H2O-019TR In distribution
H2O-010TR In distribution
610-2312, 610-2312-5 In distribution
610-214, 610-214-5 Width 3.5 cm In distribution
H2O-017TR In distribution
H2O-004TR In distribution
610-1273 Width 10.2 cm In distribution
610-1199 Length 20 cm In distribution
H2O-015TR In distribution
EA4015 Width 2.6 cm Withdrawn
610-774 Width 1.8 cm 50 Withdrawn
610-316 Width 0.94 in 100 Withdrawn
610-773 Width 1.3 cm 50 Withdrawn
UA0023 Length 20 cm Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
SonoScape Sonoscape Medical Corp. 302
Biopsy Starter Kit Civco Medical Instruments Co., Inc. 172
Sheathes Sheathing Technologies, Inc. 170
Needle Guide Civco Medical Instruments Co., Inc. 156
Sheathes3D Sheathing Technologies, Inc. 78
Ultrasound Probe Cover Biopsy Needle Guide Advance Medical Designs, Inc. 78
ultrasonic transducer Edan Instruments, Inc. 70
Unbranded Advance Medical Designs, Inc. 68
Reusable Biopsy Bracket Protek Medical Products, Inc. 60
Ultrasound Probe Cover Biopsy Needle Guide Kit Advance Medical Designs, Inc. 58
Biopsy Bracket Civco Medical Instruments Co., Inc. 56
Needle Guide Starter Kit Civco Medical Instruments Co., Inc. 52

Showing 12 of 1,678. All products under Transducer, Ultrasonic, Diagnostic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K231783 2023-11-14
K222052 2022-11-22
K211270 2021-09-13
K163313 2017-06-09
K160806 2016-08-05
K131161 2013-09-17
K131528 2013-06-11
K093713 2010-01-19
K013721 2001-12-28
K992152 1999-08-17
K991236 1999-06-02
K970513 1997-06-20
K970514 1997-06-20
K970515 1997-06-20
K843573 1984-12-13

Recalls Naming This Product

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

Recalls naming the identifiers of Transducer Cover
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Civco Medical Instruments Co., Inc. 510(k) number 2015-02-26 Class II Process design Leaks were detected in the recalled lot which may compromise the sterility of the product. 120 pouches 2017-02-28
Civco Medical Instruments Co., Inc. 510(k) number 2011-01-21 Not classified Labeling design Non-sterile transducer covers were incorrectly labeled as sterile and contained incorrect temperature storage information. 31/24-cover boxes 2013-07-09
Civco Medical Instruments Co., Inc. 510(k) number 2010-07-20 Not classified Nonconforming Material/Component Polyethylene material did not have proper treatment applied during manufacturing. Untreated polyethylene material does not maintain a secure seal with the adhesive tape used to secure the tip to the cover. 22 boxes 2012-04-13

Recalls

24 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
2025-05-01 Class II Process design During the attachment of the needle guide to the covered probe, the tight tolerance and fit of the needle guide can cause a pinhole breach in the transducer cover when latching the guide in place. 506 boxes
2018-11-02 Class II Other 613 boxes 2020-11-20
2018-11-02 Class II Other 49 boxes 2020-11-20
2018-11-02 Class II Other 66 boxes 2020-11-20
2018-11-02 Class II Other 20 boxes 2020-11-20
2018-11-02 Class II Other 234 boxes 2020-11-20
2018-11-02 Class II Other 115 boxes 2020-11-20
2018-11-02 Class II Other The needle guide bracket may puncture the sterile cover applied over the transducer and bracket during assembly. 948 boxes 2020-11-20
2018-11-02 Class II Other The needle guide bracket may puncture the sterile cover applied over the transducer and bracket during assembly. 738 boxes 2020-11-20
2018-11-02 Class II Other 73 boxes 2020-11-20
2018-11-02 Class II Other 257 boxes 2020-11-20
2018-11-02 Class II Other 468 boxes 2020-11-20
2018-11-02 Class II Other 3 boxes 2020-11-20
2018-11-02 Class II Other 297 boxes 2020-11-20
2018-11-02 Class II Other The needle guide bracket may puncture the sterile cover applied over the transducer and bracket during assembly. 1,375 boxes 2020-11-20
2018-11-02 Class II Other 135 boxes 2020-11-20
2018-07-30 Class II Process control The assembly of the needle guides were found to be either missing adhesive or did not have adequate adhesive to hold the assembled cannula in place on the needle guide. 3 units 2020-09-16
2018-07-30 Class II Process control The assembly of the needle guides were found to be either missing adhesive or did not have adequate adhesive to hold the assembled cannula in place on the needle guide. 107 units 2020-09-16
2018-02-23 Class II Device Design A cover failed leak testing during validation testing of new needle guides from a replacement tool. 177 boxes 2020-10-06
2015-10-21 Class II Process design Sterility of the product cannot be assured. 54 boxes 2017-02-28
2015-10-21 Class II Process design Sterility of the product cannot be assured. 717 boxes 2017-02-28
2015-10-21 Class II Process design Sterility of the product cannot be assured. 206 boxes 2017-02-28
2015-10-21 Class II Process design Sterility of the product cannot be assured. 1139 boxes 2017-02-28
2015-10-21 Class II Process design Sterility of the product cannot be assured. 508 boxes 2017-02-28
2008-01-16 Not classified Packaging Incorrect Needle Guide- The individual pouches contained V53W Endocavity Needle guide(p/n/034-054) instead of the Shimadzu T/R Needle guide (p/n134-054). Lot M102250 – 5 boxes; Lot M105440 – 2 boxes 2008-04-03

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