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Blank Discs

FDA UDI

Class I (US FDA UDI)

by Oxoid Limited

Identity

Trade Name
BLANK DISCS FDA UDI
Generic Name
Antibacterial susceptibility testing disc IVD FDA UDI
Model / Reference
CT0998B FDA UDI

Identifiers

Primary DI / UDI-DI
05032384007080 FDA UDI
FDA Product Code
JTO FDA UDI
GMDN Term
Antibacterial susceptibility testing disc 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: Antibacterial susceptibility testing disc IVD

Blank Discs by Oxoid Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Antibacterial susceptibility testing disc IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oxoid Limited

Sources (1)

  • FDA UDI e3cc59af-263e-4440-88ee-89f700ebd446 33 fields · synced May 31, 2026