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Refrigeration Medium - Test Yolk Buffer (TYB) with Gentamicin

FDA UDI

Class II (US FDA UDI)

by Fujifilm Irvine Scientific, Inc.

Identity

Trade Name
Refrigeration Medium - Test Yolk Buffer (TYB) with Gentamicin FDA UDI
Generic Name
IVF medium FDA UDI
Device Name
Refrigeration Test Yolk Buffer with Gentamicin FDA UDI
Model / Reference
90129-20x5mL FDA UDI
Description
Refrigeration Test Yolk Buffer with Gentamicin FDA UDI

Identifiers

Catalog Number
90129 FDA UDI
Primary DI / UDI-DI
00893727002866 FDA UDI
FDA Product Code
HDR FDA UDI
GMDN Term
IVF medium FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 5 Milliliter FDA UDI

Category: IVF medium

Refrigeration Medium - Test Yolk Buffer (TYB) with Gentamicin by Fujifilm Irvine Scientific, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as IVF medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d634ea69-f847-4df6-b0b4-be4d06a5d81c 37 fields · synced Jun 6, 2026