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Mft25 O2 Ds _ _9/16 S

FDA UDI

Class I (US FDA UDI)

by GCE, s.r.o.

Identity

Trade Name
MFT25 O2 DS _ _9/16 S FDA UDI
Generic Name
Medical gas flowmeter, Thorpe tube FDA UDI
Device Name
Mediflow devices are intended for the administration of the following medical gases in the treatment and care of patients. This flow selector is intended to be fitted to medical gas pipeline system terminal units in hospitals or ambulance cars or to a quick connector outlet of a medical gas regulator. FDA UDI
Model / Reference
0726502US FDA UDI
Description
Mediflow devices are intended for the administration of the following medical gases in the treatment and care of patients. This flow selector is intended to be fitted to medical gas pipeline system terminal units in hospitals or ambulance cars or to a quick connector outlet of a medical gas regulator. FDA UDI

Identifiers

Primary DI / UDI-DI
08592346818262 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
Not 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Mft25 O2 Ds _ _9/16 S by GCE, s.r.o. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
GCE, s.r.o.

Sources (1)

  • FDA UDI 7f633735-3f47-4811-8be0-8cb2c6798aa9 34 fields · synced Jun 8, 2026