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Remel

FDA UDI

Class I (US FDA UDI)

by Remel, Inc.

Identity

Trade Name
REMEL FDA UDI
Generic Name
Yeast species culture isolate identification/antimicrobial susceptibility profile IVD, kit FDA UDI
Device Name
Rapid Trehalose Assim Broth(0.2ml) 20/PK FDA UDI
Model / Reference
R064856 FDA UDI
Description
Rapid Trehalose Assim Broth(0.2ml) 20/PK FDA UDI

Identifiers

Catalog Number
R064856 FDA UDI
Primary DI / UDI-DI
00848838010163 FDA UDI
FDA Product Code
JXC FDA UDI
GMDN Term
Yeast species culture isolate identification/antimicrobial susceptibility profile IVD, kit 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: Yeast species culture isolate identification/antimicrobial susceptibility profile IVD, kit

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

Similar devices

Also classified as Yeast species culture isolate identification/antimicrobial susceptibility profile IVD, kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Remel, Inc.

Sources (1)

  • FDA UDI 4cf04bc7-e4dd-426d-8a48-6e36c6b385cd 34 fields · synced Jun 8, 2026