Identity
- Trade Name
- BBL EUDAMEDBD BBL™ Todd Hewitt Broth with Gentamicin and Nalidixic Acid FDA UDI
- Generic Name
- Differential/selective broth culture medium IVD FDA UDI
- Device Name
- BD BBL™ Todd Hewitt Broth with Gentamicin and Nalidixic Acid EUDAMEDBD BBL™ Todd Hewitt Broth with Gentamicin and Nalidixic Acid, Carton of 100 size K tubes FDA UDI
- Model / Reference
- 299486 EUDAMEDFDA UDI
- Description
- BD BBL™ Todd Hewitt Broth with Gentamicin and Nalidixic Acid, Carton of 100 size K tubes FDA UDI
Identifiers
- Catalog Number
- 299486 FDA UDI
- Primary DI / UDI-DI
- 30382902994863 EUDAMEDFDA UDI
- Basic UDI-DI
- 038290KKBKFOMY7F EUDAMED
- Unit of Use DI
- 00382902994862 EUDAMED
- FDA Product Code
- JSG FDA UDI
- EMDN Code
- W0104010206 MEDIA IN TUBES (SOLID & LIQUID) EUDAMED
- GMDN Term
- Differential/selective broth culture medium IVD FDA UDI
Classification
- Device Class
- Class A EUDAMEDClass I FDA UDI
- Regulation Number
- 866.2300 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
Yes
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
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 — 5 Milliliter FDA UDI
Bbl by Becton, Dickinson and Company — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/IVDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 038290KKBKFOMY7F | Class A | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Becton, Dickinson and Company
- EUDAMED SRN
- US-MF-000018910
- Authorised Representative
- Becton Dickinson Ireland Limited IE-AR-000007610
Sources (2)
- EUDAMED 214fe669-7297-4c27-b4ac-993ed0c78455 61 fields · synced Jun 9, 2026
- FDA UDI c69f19b4-cd77-4124-a437-0902ceff0c18 37 fields · synced May 30, 2026