Identity
- Trade Name
- BD BACTEC™ Plus Aerobic/F Culture Vials FDA UDI
- Generic Name
- Culture medium antimicrobial supplement IVD FDA UDI
- Device Name
- BD BACTEC™ Plus Aerobic/F Medium FDA UDI
- Model / Reference
- 442023 FDA UDI
- Description
- BD BACTEC™ Plus Aerobic/F Medium FDA UDI
Identifiers
- Catalog Number
- 442023 FDA UDI
- Primary DI / UDI-DI
- 00382904420239 FDA UDI
- FDA Product Code
- MDB FDA UDI
- GMDN Term
- Culture medium antimicrobial supplement IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 866.2560 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
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
Yes
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
Dimensions & Sizes
- Size
- Total Volume — 30 Milliliter FDA UDI
Category: Culture medium antimicrobial supplement IVD
BD BACTEC™ Plus Aerobic/F Culture Vials by Becton Dickinson And Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 11e681b5-f55c-4a2b-abc2-3c91cc3ab1de 38 fields · synced May 30, 2026