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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Medical gas flowmeter, dial-type FDA UDI
Device Name
FLOWMETER,OXY,BRASS,8L,DISS NUT/NIPPLE FDA UDI
Model / Reference
RTFMO8LDN FDA UDI
Description
FLOWMETER,OXY,BRASS,8L,DISS NUT/NIPPLE FDA UDI

Identifiers

Catalog Number
RTFMO8LDN FDA UDI
Primary DI / UDI-DI
10193489104103 FDA UDI
FDA Product Code
CAX FDA UDI
GMDN Term
Medical gas flowmeter, dial-type 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical gas flowmeter, dial-type

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

Similar devices

Also classified as Medical gas flowmeter, dial-type.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4bdf493a-431b-4315-b90f-2818cf5ead4a 35 fields · synced Jun 1, 2026