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The Harris Products Group

FDA UDI

Class I (US FDA UDI)

by J. W. Harris Co., Inc.

Identity

Trade Name
The Harris Products Group FDA UDI
Generic Name
Medical air cylinder regulator FDA UDI
Model / Reference
FLWMTR,FME201 02-8 LPM W/O INLET FDA UDI

Identifiers

Catalog Number
3500649 FDA UDI
Primary DI / UDI-DI
00850005066323 FDA UDI
FDA Product Code
CAX FDA UDI
GMDN Term
Medical air cylinder regulator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.2340 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical air cylinder regulator

The Harris Products Group by J. W. Harris Co., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical air cylinder regulator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
J. W. Harris Co., Inc.

Sources (1)

  • FDA UDI 7aa24259-f870-4531-bf3f-addc6e108101 33 fields · synced May 30, 2026