← Back to catalogue

Remel

FDA UDI

Class I (US FDA UDI)

by Remel, Inc.

Identity

Trade Name
REMEL FDA UDI
Generic Name
Anaerobic-microorganism antimicrobial susceptibility culture medium IVD FDA UDI
Device Name
Anaer (CDC) Blood Agar 100/PK FDA UDI
Model / Reference
R01036 FDA UDI
Description
Anaer (CDC) Blood Agar 100/PK FDA UDI

Identifiers

Catalog Number
R01036 FDA UDI
Primary DI / UDI-DI
00848838000003 FDA UDI
FDA Product Code
JSG FDA UDI
GMDN Term
Anaerobic-microorganism antimicrobial susceptibility culture medium IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2300 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: Anaerobic-microorganism antimicrobial susceptibility culture medium IVD

Remel by Remel, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaerobic-microorganism antimicrobial susceptibility culture medium IVD.

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

Manufacturer
Remel, Inc.

Sources (1)

  • FDA UDI c62c7270-fabb-4799-9974-0efccddd3e85 34 fields · synced May 31, 2026