Identity
- Trade Name
- BD Difco™ QC Antigen Shigella Group A FDA UDI
- Generic Name
- Multiple Shigella species culture isolate antigen IVD, control FDA UDI
- Device Name
- Vial Qc Antigen Shigella Grp A 1Ml FDA UDI
- Model / Reference
- 221001 FDA UDI
- Description
- Vial Qc Antigen Shigella Grp A 1Ml FDA UDI
Identifiers
- Catalog Number
- 221001 FDA UDI
- Primary DI / UDI-DI
- 00382902210016 FDA UDI
- FDA Product Code
- LIA FDA UDI
- GMDN Term
- Multiple Shigella species culture isolate antigen IVD, control FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.3660 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
Dimensions & Sizes
- Size
- Total Volume — 1 Milliliter FDA UDI
BD Difco™ QC Antigen Shigella Group A by Becton Dickinson And Company — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Becton Dickinson And Company
Sources (1)
- FDA UDI eb809b80-1c40-43db-b531-1a5b37e64978 38 fields · synced Jun 1, 2026