InteliQ

InteliQ Diabetes Control Trilevel MiniPak (A human whole blood assayed diabetes control.)

Registry build 21.09.26
2manufacturers in China registered for this device type
4catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Zhejiang (1), Guangxi (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code GGM
Manufacturer City Province Registered as Device types
Acon Biotech (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 29
Urit Medical Electronic Co., Ltd. Guilin Guangxi Contract manufacturer 28

Record

Regulatory record for InteliQ
Listed by Bio-Rad Laboratories Inc., United States
FDA product code GGM
Device type Control, Hemoglobin
Device class Class 2
Regulation 21 CFR 864.8625
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2021-04-30
Record revised 2023-01-31 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature -70 to -20 °C

Catalogue Numbers

Catalogue numbers for InteliQ
Catalogue number Size Status
12008311 In distribution
12008310 In distribution
12008312 In distribution
12008309 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Eurotrol Eurotrol B.V. 11
CueSee® Co-OX Eurotrol B.V. 11
Research and Diagnostic Systems Research AND Diagnostic Systems, Inc. 10
Liquichek Bio-Rad Laboratories Inc. 8
Hemoglobin Test Strip Urit Medical Electronic Co., Ltd. 3
HemoTrol Duo Eurotrol B.V. 3
Lyphochek Bio-Rad Laboratories Inc. 3
McKesson Mckesson Medical-Surgical Inc. 3
HemoTrol WB Eurotrol B.V. 3
Hemoglobin Control Solution Urit Medical Electronic Co., Ltd. 3
Hemoglobin Meter Urit Medical Electronic Co., Ltd. 2
Henry Schein Henry Schein, Inc. 1

Showing 12 of 25. All products under Control, Hemoglobin

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K070546 2007-04-02

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