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BD Phoenix™ Inoculum Broth

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Phoenix™ Inoculum Broth FDA UDI
Generic Name
Buffered isotonic saline reagent IVD FDA UDI
Device Name
BD Phoenix™ Inoculum Broth FDA UDI
Model / Reference
246005 FDA UDI
Description
BD Phoenix™ Inoculum Broth FDA UDI

Identifiers

Catalog Number
246005 FDA UDI
Primary DI / UDI-DI
30382902460054 FDA UDI
FDA Product Code
JSG FDA UDI
GMDN Term
Buffered isotonic saline reagent IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2300 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

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

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 — 2.2 Milliliter FDA UDI

Category: Buffered isotonic saline reagent IVD

BD Phoenix™ Inoculum Broth by Becton Dickinson And Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Buffered isotonic saline reagent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b39695c0-5a41-4e4a-91e4-e70dfc209999 37 fields · synced Jun 6, 2026