← Back to catalogue

BD PhoenixSpec™ Nephelometer

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD PhoenixSpec™ Nephelometer FDA UDI
Generic Name
Microorganism-density nephelometer IVD FDA UDI
Device Name
BD PhoenixSpec™ Nephelometer FDA UDI
Model / Reference
440910 FDA UDI
Description
BD PhoenixSpec™ Nephelometer FDA UDI

Identifiers

Catalog Number
440910 FDA UDI
Primary DI / UDI-DI
00382904409104 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 7.87 Inch FDA UDI
Length — 13.62 Inch FDA UDI
Height — 5.75 Inch FDA UDI

Category: Microorganism-density nephelometer IVD

BD PhoenixSpec™ Nephelometer by Becton Dickinson And Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microorganism-density nephelometer IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Becton Dickinson And Company

Sources (1)

  • FDA UDI c271fa07-285a-4091-851d-9a5c8ebc5511 36 fields · synced Jun 1, 2026