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Genemed®

FDA UDI

Class I (US FDA UDI)

by Sakura Finetek USA, Inc

Identity

Trade Name
Genemed® FDA UDI
Generic Name
Streptavidin-enzyme conjugate reagent IVD FDA UDI
Device Name
Acu-Stain™ HRP Kit for Mouse + Rabbit, 125 mL each FDA UDI
Model / Reference
54-0003 FDA UDI
Description
Acu-Stain™ HRP Kit for Mouse + Rabbit, 125 mL each FDA UDI

Identifiers

Catalog Number
54-0003 FDA UDI
Primary DI / UDI-DI
00615233005618 FDA UDI
FDA Product Code
PPM FDA UDI
GMDN Term
Streptavidin-enzyme conjugate reagent IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4010 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

Yes

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

Yes

FDA UDI

Category: Streptavidin-enzyme conjugate reagent IVD

Genemed® by Sakura Finetek USA, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Streptavidin-enzyme conjugate reagent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 47901508-3a84-43dc-99f7-0fe7172acde6 35 fields · synced Jun 8, 2026