← Back to catalogue

BD BBL™ Bio-Bag™ Environmental Chamber Type C

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD BBL™ Bio-Bag™ Environmental Chamber Type C FDA UDI
Generic Name
Atmospheric generation kit IVD FDA UDI
Device Name
Bag Bio-Bag Type Cfj 25 Ea FDA UDI
Model / Reference
261212 FDA UDI
Description
Bag Bio-Bag Type Cfj 25 Ea FDA UDI

Identifiers

Catalog Number
261212 FDA UDI
Primary DI / UDI-DI
30382902612125 FDA UDI
FDA Product Code
KZJ FDA UDI
GMDN Term
Atmospheric generation kit IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2580 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

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

BD BBL™ Bio-Bag™ Environmental Chamber Type C 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

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

Manufacturer

Sources (1)

  • FDA UDI 755f1c5c-f9cf-430f-9ce4-0984bd01bd70 37 fields · synced May 30, 2026