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Linde

FDA UDI

Class I (US FDA UDI)

by Western Enterprises, Inc.

Identity

Trade Name
Linde FDA UDI
Generic Name
Fixed medical gas cylinder regulator FDA UDI
Device Name
PRAXAIR 1-KNOB VIPR "D" CYL FDA UDI
Model / Reference
PRX-9632 FDA UDI
Description
PRAXAIR 1-KNOB VIPR "D" CYL FDA UDI

Identifiers

Catalog Number
PRX-9632 FDA UDI
Primary DI / UDI-DI
B929PRX96320 FDA UDI
FDA Product Code
CAN FDA UDI
GMDN Term
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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Fixed medical gas cylinder regulator

Linde by Western Enterprises, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as 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 9b55edd1-de83-4597-a8c2-f7e9145d8535 34 fields · synced Jun 7, 2026