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An-Ident Discsdd6 6x50 Discs

FDA UDI

Class I (US FDA UDI)

by Oxoid Limited

Identity

Trade Name
AN-IDENT DISCSDD6 6X50 DISCS FDA UDI
Generic Name
Multiple antimycobacterial susceptibility testing kit IVD FDA UDI
Model / Reference
DD0006A FDA UDI

Identifiers

Primary DI / UDI-DI
05032384007189 FDA UDI
FDA Product Code
JTO FDA UDI
GMDN Term
Multiple antimycobacterial susceptibility testing kit IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2660 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

No

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

Category: Multiple antimycobacterial susceptibility testing kit IVD

An-Ident Discsdd6 6x50 Discs by Oxoid Limited — Class I — 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

Manufacturer
Oxoid Limited

Sources (1)

  • FDA UDI ffc34725-c930-4094-be8f-399abbdfd440 32 fields · synced Jun 8, 2026