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QuSTICK™ Strep A

FDA UDI

Class I (US FDA UDI)

by Stanbio Laboratory, L.p.

Identity

Trade Name
QuSTICK™ Strep A FDA UDI
Generic Name
Beta-haemolytic Group A Streptococcus antigen IVD, kit, rapid ICT, clinical FDA UDI
Device Name
A rapid test for the qualitative detection of Strep A antigen in throat swab specimens. FDA UDI
Model / Reference
6000-025 FDA UDI
Description
A rapid test for the qualitative detection of Strep A antigen in throat swab specimens. FDA UDI

Identifiers

Catalog Number
6000-025 FDA UDI
Primary DI / UDI-DI
00657498600016 FDA UDI
FDA Product Code
GTY FDA UDI
GMDN Term
Beta-haemolytic Group A Streptococcus antigen IVD, kit, rapid ICT, clinical 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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 Group A Streptococcus antigen IVD, kit, rapid ICT, clinical

QuSTICK™ Strep A by Stanbio Laboratory, L.p. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Beta-haemolytic Group A Streptococcus antigen IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 41fb6b03-00b5-41b0-a757-57369b5b56a7 36 fields · synced May 31, 2026