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chromID™ Candida Agar

FDA UDI

Class I (US FDA UDI)

by Biomerieux , Inc.

Identity

Trade Name
chromID™ Candida Agar FDA UDI
Generic Name
Differential/selective agar culture medium IVD FDA UDI
Device Name
Chromogenic medium for the selective isolation of yeasts and the direct identification of Candida albicans FDA UDI
Model / Reference
chromID™ Candida Agar FDA UDI
Description
Chromogenic medium for the selective isolation of yeasts and the direct identification of Candida albicans FDA UDI

Identifiers

Primary DI / UDI-DI
03573026599812 FDA UDI
FDA Product Code
JSI FDA UDI
GMDN Term
Differential/selective agar culture medium IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2360 FDA UDI
Commercial Distribution
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

Category: Differential/selective agar culture medium IVD

chromID™ Candida Agar by Biomerieux , Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Differential/selective agar culture medium IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomerieux , Inc.

Sources (1)

  • FDA UDI 1a54c77e-b50f-42cf-8eb6-a20e8755c75f 34 fields · synced May 30, 2026