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Gems Geri Medium

FDA UDI

Class II (US FDA UDI)

by Genea Biomedx Pty Ltd

Identity

Trade Name
Gems Geri Medium FDA UDI
Generic Name
IVF medium FDA UDI
Device Name
The Gems Geri Medium is intended for culture of embryos from fertilization to blastulation stage and transfer of embryos to the uterus. FDA UDI
Model / Reference
ONE-50 FDA UDI
Description
The Gems Geri Medium is intended for culture of embryos from fertilization to blastulation stage and transfer of embryos to the uterus. FDA UDI

Identifiers

Primary DI / UDI-DI
09348265005035 FDA UDI
510(k) Number
K161261 FDA UDI
FDA Product Code
MQL FDA UDI
GMDN Term
IVF medium FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.6180 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

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 50 Milliliter FDA UDI

Category: IVF medium

Gems Geri Medium by Genea Biomedx Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as IVF medium.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 65a87945-69f5-40e7-8edf-f52b7d4e1e32 36 fields · synced Jun 8, 2026