Reusable Stainless Steel Endocavity Needle Guide

Stainless Steel Reusable Endocavity Needle Guide for GE RIC5-9-D, RIC5-9H, RIC5-9W-D, RIC5-9W-RS, & RIC6-12-D, Mindray DE10-3U and Samsung Medison V5-9 Ultrasound Transducers

Registry build 21.09.26
44manufacturers in China registered for this device type
43catalogue numbers in this listing
5510(k) clearances naming this product 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 Reusable Stainless Steel Endocavity Needle Guide
Listed by Protek Medical Products, Inc., United States
FDA product code ITX
Device type Transducer, Ultrasonic, Diagnostic
Device class Class 2
Regulation 21 CFR 892.1570
510(k) K971115
Record published 2016-09-16
Record revised 2022-06-17 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Reusable Stainless Steel Endocavity Needle Guide
Catalogue number Size Status
6191 In distribution
6482 In distribution
6256 In distribution
6098 In distribution
6076 In distribution
6131 In distribution
6267 In distribution
6360 In distribution
6531 In distribution
6095 In distribution
6391 In distribution
6433 In distribution
6182 In distribution
6477 In distribution
6097 In distribution
6467 In distribution
6341 In distribution
6382 In distribution
6449 In distribution
6174 In distribution
6078 In distribution
6019 In distribution
6006 In distribution
6190 In distribution
6550 In distribution
6042 In distribution
6268 In distribution
6045 In distribution
6381 In distribution
6116 In distribution
6478 In distribution
6005 In distribution
6340 In distribution
6077 In distribution
6455 In distribution
6043 In distribution
6194 In distribution
6370 In distribution
6392 In distribution
6532 In distribution
6026 In distribution
6476 In distribution
6448 In distribution

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
Transducer Cover Civco Medical Instruments Co., Inc. 54

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
K973958 1998-01-22
K973622 1997-11-26
K973362 1997-10-01
K971722 1997-07-10
K971115 1997-06-13

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