Identity
- Trade Name
- BD PhoenixSpec™ AP Calibrator Kit FDA UDI
- Generic Name
- Microorganism-density nephelometer IVD FDA UDI
- Device Name
- BD PhoenixSpec™ AP Calibrator Kit FDA UDI
- Model / Reference
- 441951 FDA UDI
- Description
- BD PhoenixSpec™ AP Calibrator Kit FDA UDI
Identifiers
- Catalog Number
- 441951 FDA UDI
- Primary DI / UDI-DI
- 00382904419516 FDA UDI
- FDA Product Code
- JQX FDA UDI
- GMDN Term
- Microorganism-density nephelometer IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.2700 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Category: Microorganism-density nephelometer IVD
BD PhoenixSpec™ AP Calibrator Kit by Becton Dickinson And Company — Class I — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Microorganism-density nephelometer IVD.
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
IVDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | IVDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Becton Dickinson And Company
Sources (2)
- FDA UDI fdd7ae44-ec43-40ab-b5bd-866bad0277de 36 fields · synced Jun 19, 2026
- EUDAMED 1 fields · synced May 29, 2026