Identity
- Trade Name
- BD Difco™ FA Bordetella Pertussis Antiserum FDA UDI
- Generic Name
- Multiple Bordetella species antigen IVD, kit, fluorescent immunoassay FDA UDI
- Device Name
- Vial Fa Bordetella Pertussis 5Ml FDA UDI
- Model / Reference
- 223591 FDA UDI
- Description
- Vial Fa Bordetella Pertussis 5Ml FDA UDI
Identifiers
- Catalog Number
- 223591 FDA UDI
- Primary DI / UDI-DI
- 00382902235910 FDA UDI
- FDA Product Code
- GOZ FDA UDI
- GMDN Term
- Multiple Bordetella species antigen IVD, kit, fluorescent immunoassay FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 866.3065 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
BD Difco™ FA Bordetella Pertussis Antiserum by Becton Dickinson And Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Becton Dickinson And Company
Sources (1)
- FDA UDI 5d989de5-606a-4e5a-8e11-9f1bad0ad4b5 37 fields · synced Jun 6, 2026