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Gynex

FDA UDI

Class I (US FDA UDI)

by Gynex Corporation

Identity

Trade Name
Gynex FDA UDI
Generic Name
Gel warmer FDA UDI
Model / Reference
D82-01 FDA UDI

Identifiers

Primary DI / UDI-DI
GYNXD82010 FDA UDI
FDA Product Code
IRQ FDA UDI
GMDN Term
Gel warmer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5950 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Gel warmer

Gynex by Gynex Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gel warmer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gynex Corporation

Sources (1)

  • FDA UDI e51a792a-2564-4c00-9c66-1961e5cfbda4 32 fields · synced Jun 6, 2026