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Precision Medical Inc

FDA UDI

Class I (US FDA UDI)

by Precision Medical, Inc.

Identity

Trade Name
Precision Medical Inc FDA UDI
Generic Name
Medical gas flowmeter, Thorpe tube FDA UDI
Device Name
1MFA Series Oxygen Flowmeter - Manufactured for TriTech Medical Inc. FDA UDI
Model / Reference
1MFA Series Oxygen Flowmeter - TriTech Medical Inc. FDA UDI
Description
1MFA Series Oxygen Flowmeter - Manufactured for TriTech Medical Inc. FDA UDI

Identifiers

Primary DI / UDI-DI
00855887006894 FDA UDI
FDA Product Code
CAX FDA UDI
GMDN Term
Medical gas flowmeter, Thorpe tube 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical gas flowmeter, Thorpe tube

Precision Medical Inc by Precision Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical gas flowmeter, Thorpe tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d526d4e5-e692-460b-8134-de77d334468e 34 fields · synced Jun 8, 2026