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Prolex Streptococcal- Select Grouping Latex Kit

FDA UDI

Class I (US FDA UDI)

by Pro-Lab, Incorporated

Identity

Trade Name
Prolex Streptococcal- Select Grouping Latex Kit FDA UDI
Generic Name
Beta-haemolytic Streptococcus serological grouping IVD, kit, agglutination FDA UDI
Device Name
Any combination of six Latex Reagents for Lancefield Groups A, B, C, D, F, and G. FDA UDI
Model / Reference
PL.041 FDA UDI
Description
Any combination of six Latex Reagents for Lancefield Groups A, B, C, D, F, and G. FDA UDI

Identifiers

Catalog Number
PL.041 FDA UDI
Primary DI / UDI-DI
10628429000295 FDA UDI
FDA Product Code
GTZ FDA UDI
GMDN Term
Beta-haemolytic Streptococcus serological grouping IVD, kit, agglutination FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Beta-haemolytic Streptococcus serological grouping IVD, kit, agglutination

Prolex Streptococcal- Select Grouping Latex Kit by Pro-Lab, Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Beta-haemolytic Streptococcus serological grouping IVD, kit, agglutination.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 76b8edd7-a090-41d0-b8fc-adc1d0c716d3 34 fields · synced Jun 8, 2026