GEM Flow Coupler External Lead

An external lead that joins the FLOW COUPLER probe to the FLOW COUPLER Monitor

Registry build 21.09.26
4manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

All of them in Guangdong.

Chinese manufacturers registered for FDA product code DPW
Manufacturer City Province Registered as Device types
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Helen of Troy Macao Limited Macau Guangdong Private-label distributor 11
Dongguan Mars Medical Products Co., Ltd. Dongguan Guangdong Manufacturer 9
Onbo Electronic (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 6

Record

Regulatory record for GEM Flow Coupler External Lead
Listed by Synovis Micro Companies Alliance, United States
FDA product code DPW
Device type Flowmeter, Blood, Cardiovascular
Device class Class 2
Regulation 21 CFR 870.2100
510(k) K093310
Record published 2016-09-24
Record revised 2023-07-20 (version 6)

Specifications

Specifications
MRI safety MR Unsafe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Storage Storage environment temperature 20 to 25 °C; Storage environment temperature 68 to 77 °F
Packaging Case of 4

Catalogue Numbers

Catalogue numbers for GEM Flow Coupler External Lead
Catalogue number Size Status
GEM1003EXT-FC In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Transonic Transonic Systems, Inc. 627
SonoTT Vascular Probe Em-Tec GmbH 12
BiDop 7 probe Koven Technology, Inc. 8
Medistim MiraQ Cardiac System Medistim ASA 6
Medistim MiraQ Vascular System Medistim ASA 6
FlowMet™ Medtronic, Inc. 4
GEM Flow Coupler Synovis Micro Companies Alliance 4
CooperSurgical® Coopersurgical, Inc. 4
Medistim System Activation Card Medistim ASA 3
811-BL 24V Foreign & Domestic Parks Medical Electronics, Inc. 3
Medistim MiraQ Ultimate System Medistim ASA 3
Dopplex Huntleigh Healthcare Ltd. 3

Showing 12 of 154. All products under Flowmeter, Blood, Cardiovascular

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K213974 2022-04-20

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