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BD Difco™ QC Antigen Shigella Group C1

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Difco™ QC Antigen Shigella Group C1 FDA UDI
Generic Name
Multiple Shigella species culture isolate antigen IVD, control FDA UDI
Device Name
Vial Qc Antigen Shigella Grp C1 1Ml FDA UDI
Model / Reference
221041 FDA UDI
Description
Vial Qc Antigen Shigella Grp C1 1Ml FDA UDI

Identifiers

Catalog Number
221041 FDA UDI
Primary DI / UDI-DI
00382902210412 FDA UDI
FDA Product Code
LIA FDA UDI
GMDN Term
Multiple Shigella species culture isolate antigen IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3660 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

Yes

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 — 1 Milliliter FDA UDI

BD Difco™ QC Antigen Shigella Group C1 by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 04802d37-d889-4443-8896-d7b2c6bcbf50 38 fields · synced May 30, 2026