Identity
- Trade Name
- BioStrep® A FDA UDI
- Generic Name
- Beta-haemolytic Group A Streptococcus antigen IVD, kit, rapid ICT, clinical FDA UDI
- Device Name
- BioStrep® A strip; 30 Test kit; CE FDA UDI
- Model / Reference
- BSP-185-30-04 FDA UDI
- Description
- BioStrep® A strip; 30 Test kit; CE FDA UDI
Identifiers
- Catalog Number
- BSP-185-30-04 FDA UDI
- Primary DI / UDI-DI
- 10743816000891 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
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 Group A Streptococcus antigen IVD, kit, rapid ICT, clinical
BioStrep® A by Princeton Biomeditech Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Beta-haemolytic Group A Streptococcus antigen IVD, kit, rapid ICT, clinical.
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- McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class I
- BD Veritor™ System for Rapid Detection of Group A Strep CLIA-Waived Kit — BECTON DICKINSON AND COMPANY · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Princeton Biomeditech Corp.
Sources (1)
- FDA UDI ef95bed8-df6e-49fc-937e-59cda04319a5 36 fields · synced Jun 1, 2026