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Gentec®

FDA UDI

Class I (US FDA UDI)

by Gentec(shanghai)corporation

Identity

Trade Name
GENTEC® FDA UDI
Generic Name
Non-fixed medical gas cylinder regulator FDA UDI
Device Name
195M Series, Medical Gas Regulator, Oxygen,Air,N2O,CO2, Brass FDA UDI
Model / Reference
195M Series FDA UDI
Description
195M Series, Medical Gas Regulator, Oxygen,Air,N2O,CO2, Brass FDA UDI

Identifiers

Primary DI / UDI-DI
06970966663387 FDA UDI
FDA Product Code
CAN FDA UDI
GMDN Term
Non-fixed medical gas cylinder regulator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.2700 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Non-fixed medical gas cylinder regulator

Gentec® by Gentec(shanghai)corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-fixed medical gas cylinder regulator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f3770cf2-0df3-4c85-b10b-47a14c9cefff 34 fields · synced Jun 1, 2026