FetaLink

9 catalogue numbers from FetaLink 200, listed by Cerner Corporation, United States, under System, Monitoring, Perinatal. 6 manufacturers in China are registered for this product code.

Registry build 21.09.26
6manufacturers in China registered for this device type
9catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (4), Jiangsu (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 HGM
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Luen Hing Textile -Shangyu Manufacturing(ZHONG Shan) Co Ltd Zhongshan Guangdong Contract manufacturer 2
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Orantech Inc. Shenzhen Guangdong Contract manufacturer 40
China Qingdao Bright Medical Manufacturing Co., Ltd. Qingdao Shandong Contract manufacturer 8

Record

Regulatory record for FetaLink
Listed by Cerner Corporation, United States
FDA product code HGM
Device type System, Monitoring, Perinatal
Device class Class 2
Regulation 21 CFR 884.2740
Establishment Complaint-file establishment, Manufacturer
510(k) K091251
Record published 2025-04-21
Record revised 2025-04-22 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, serial number
Distribution end date 2021-03-01

Catalogue Numbers

Catalogue numbers for FetaLink
Catalogue number Size Status
FetaLink 200 In distribution
FetaLink+5 In distribution
FetaLink+6 In distribution
FetaLink+3 In distribution
FL+Android1 In distribution
FL+7 In distribution
FetaLink+4 In distribution
FetaLink2013 Withdrawn
FetaLink2014 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
R&D Batteries, Inc. R & D Batteries, Inc. 137
Sonicaid Huntleigh Healthcare Ltd. 39
Obix Huntleigh Healthcare Ltd. 33
Ameritus Transducer Kentec Medical, LLC 28
Fetal Monitor Remote Display Clinicomp Intl., Inc. 18
Tenacore Tenacore LLC 11
PeriWatch Vigilance® HUB™ PeriGen Solutions Ltd. 9
Dopplex Huntleigh Healthcare Ltd. 9
Mini Telemetry System Wipro GE Healthcare Private Ltd. 8
Natus Neurology Natus Neurology Incorporated 8
Fetal & maternal monitor Edan Instruments, Inc. 8
PeriWatch Vigilance® Curve™ PeriGen Solutions Ltd. 8

Showing 12 of 117. All products under System, Monitoring, Perinatal

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K121758 2012-10-09
K091251 2009-08-25

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