Prolex E. Coli O111 Latex Reagent

Catalogue number PL.1074, listed by pro-lab incorporated, Canada, under Antisera, All Types, Escherichia Coli. 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
1510(k) clearance

Who Else Makes It

All of them in Jilin.

Chinese manufacturers registered for FDA product code GNA
Manufacturer City Province Registered as Device types
Changchun Wancheng BIO-Electron Co., Ltd. Changchun Jilin Contract manufacturer 34
Changchun Merydi BIO-Tech Co., Ltd. Changchun Jilin Manufacturer 24
Jilin Hongyi BIO-Tech Co., Ltd. Changchun Jilin Manufacturer 24

Record

Regulatory record for Prolex E. coli O111 Latex Reagent
Listed by pro-lab incorporated, Canada
FDA product code GNA
Device type Antisera, All Types, Escherichia Coli
Device class Class 1
Regulation 21 CFR 866.3255
Establishment Contract manufacturer, Manufacturer, Exporter
Premarket notification Exempt
Record published 2022-12-26

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Prolex E. coli O111 Latex Reagent
Catalogue number Size Status
PL.1074 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Mast Assure Antisera Mast Group Ltd. 7
E. coli O134 serum high titer, 1 mL SSI Diagnostica A/S 2
E. coli O73 serum high titer, 1 mL SSI Diagnostica A/S 1
E. coli O25 serum, 1 mL SSI Diagnostica A/S 1
E. coli O89 serum high titer, 1 mL SSI Diagnostica A/S 1
ImmuLex E. coli O55, 1.5 mL SSI Diagnostica A/S 1
E. coli O60 serum, 1 mL SSI Diagnostica A/S 1
E. coli O10 serum high titer, 1 mL SSI Diagnostica A/S 1
E. coli O110 serum, 1 mL SSI Diagnostica A/S 1
E. coli O88 serum high titer, 1 mL SSI Diagnostica A/S 1
E. coli O147 serum, 1 mL SSI Diagnostica A/S 1
E. coli OK O55 serum, 3 mL SSI Diagnostica A/S 1

Showing 12 of 492. All products under Antisera, All Types, Escherichia Coli

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K903714 1991-01-24

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