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BD Phoenix™ Automated Microbiology System, Remanufactured

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Phoenix™ Automated Microbiology System, Remanufactured FDA UDI
Generic Name
Microorganism identification/antimicrobial-susceptibility analyser IVD FDA UDI
Device Name
BD Phoenix™ Automated Microbiology System, Remanufactured FDA UDI
Model / Reference
448105 FDA UDI
Description
BD Phoenix™ Automated Microbiology System, Remanufactured FDA UDI

Identifiers

Catalog Number
448105 FDA UDI
Primary DI / UDI-DI
00382904481056 FDA UDI
FDA Product Code
LON FDA UDI
GMDN Term
Microorganism identification/antimicrobial-susceptibility analyser IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.1645 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Depth — 29.5 Inch FDA UDI
Height — 41.7 Inch FDA UDI
Width — 44.3 Inch FDA UDI

BD Phoenix™ Automated Microbiology System, Remanufactured by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Becton Dickinson And Company

Sources (1)

  • FDA UDI 47a63cb9-6f30-4d58-90c1-927c82d7d5fa 38 fields · synced Jun 8, 2026