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Manifold

FDA UDI

Class I (US FDA UDI)

by Maxtec, Inc.

Identity

Trade Name
Manifold FDA UDI
Generic Name
Medical gas flowmeter, Thorpe tube FDA UDI
Device Name
Manifold, 0-70 and 2-26 LPM Dual Thorpe Flowmeter with DISS Fitting and Hose FDA UDI
Model / Reference
0-70 and 2-26 LPM Dual Thorpe FDA UDI
Description
Manifold, 0-70 and 2-26 LPM Dual Thorpe Flowmeter with DISS Fitting and Hose FDA UDI

Identifiers

Catalog Number
R220P10-002 FDA UDI
Primary DI / UDI-DI
00817770023869 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medical gas flowmeter, Thorpe tube

Manifold by Maxtec, 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

Manufacturer
Maxtec, Inc.

Sources (1)

  • FDA UDI ddfbaff0-c05e-4613-aa46-7c365127d753 34 fields · synced Jun 1, 2026