Precimat Fructosamine

Catalogue number 11098993122, listed by Roche Diagnostics Gmbh, Germany, under Assay, Glycosylated Hemoglobin. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
5510(k) clearances naming this product code
3recalls on this code

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (1).

Chinese manufacturers registered for FDA product code LCP
Manufacturer City Province Registered as Device types
Wuxi Biohermes BIO & Medical Technology Co., Ltd. Wuxi Jiangsu Manufacturer 3
Shanghai Medconn Medical Technology Co., Ltd. Shanghai Shanghai Manufacturer 2
Shanghai Medconn Biotechnology Co., Ltd. Jinshan District Shanghai Manufacturer 2

Record

Regulatory record for Precimat Fructosamine
Listed by Roche Diagnostics Gmbh, Germany
FDA product code LCP
Device type Assay, Glycosylated Hemoglobin
Device class Class 2
Regulation 21 CFR 864.7470
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter
510(k) K913614
Record published 2016-09-20
Record revised 2020-12-21 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 8 °C

Catalogue Numbers

Catalogue numbers for Precimat Fructosamine
Catalogue number Size Status
11098993122 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Trinity Biotech Primus Corp. 36
Variant II Turbo Bio-Rad Laboratories Inc. 15
Pointe Scientific, Inc. Horiba Instruments Incorporated 11
Variant II Turbo Link Bio-Rad Laboratories Inc. 7
D-10 Bio-Rad Laboratories Inc. 7
Variant II Hemoglobin A1c Bio-Rad Laboratories Inc. 5
Drew Scientific Drew Scientific, Ltd. 5
Tosoh Automated Glycohemoglobin Analyzer HLC-723GR01 Tosoh Corp. 4
D-100 Bio-Rad Laboratories Inc. 4
Fructosamine Roche Diagnostics Gmbh 4
D-10 Dual Bio-Rad Laboratories Inc. 3
JAS Diagnostics Drew Scientific, Ltd. 3

Showing 12 of 134. All products under Assay, Glycosylated Hemoglobin

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K110313 2011-12-23
K072714 2008-04-18
K052464 2005-09-30
K003120 2000-12-18
K990992 1999-09-30

Recalls

The FDA has not published a severity grade for these. 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
2005-02-15 Not classified Other The product is not uniform across the cassettes of some lots, which will result in an inconsistent bias of patient results. 1800 kits. 2005-05-17
2005-02-15 Not classified Other The product is not uniform across the cassettes of some lots, which will result in an inconsistent bias of patient results. 1800 kits. 2005-05-17
2005-02-15 Not classified Other The product is not uniform across the cassettes of some lots, which will result in an inconsistent bias of patient results. 347,000 cassettes 2005-05-17

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