Identity
- Trade Name
- BD MAX™ TNA MMK FDA UDI
- Generic Name
- Nucleic acid amplification mastermix reagent IVD FDA UDI
- Device Name
- Kit BD MAX TNA MMK FDA UDI
- Model / Reference
- 442845 FDA UDI
- Description
- Kit BD MAX TNA MMK FDA UDI
Identifiers
- Catalog Number
- 442845 FDA UDI
- Primary DI / UDI-DI
- 00382904428457 FDA UDI
- FDA Product Code
- PPM FDA UDI
- GMDN Term
- Nucleic acid amplification mastermix reagent IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.4010 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
No
FDA UDI
Prescription Use
Yes
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
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 Max™ Tna Mmk 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 fc2d1d3c-960c-4708-b76a-9f42a83db5b1 37 fields · synced May 31, 2026