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1mfa Series Flowmeters (oxygen

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 1MFA Series FlowmeterModel 1MFA O2 Series Flowmeter

by Precision Medical Inc

Identity

Trade Name
1MFA SERIES FLOWMETERS (OXYGEN EUDAMED
1MFA Flowmeters FDA UDI
Generic Name
Medical gas flowmeter, Thorpe tube FDA UDI
Device Name
1MFA Flowmeter (OXYGEN) EUDAMED
1MFA SERIES FLOWMETERS (OXYGEN) FDA UDI
Model / Reference
1MFA O2 Series Flowmeter EUDAMED
1MFA Series Flowmeter EUDAMED
1MFA O2 Series FDA UDI
Description
1MFA SERIES FLOWMETERS (OXYGEN) FDA UDI

Identifiers

Primary DI / UDI-DI
00855887006740 EUDAMEDFDA UDI
Basic UDI-DI
B-00855887006740 EUDAMED
FDA Product Code
CAX FDA UDI
EMDN Code
R9099 RESPIRATORY AND ANAESTHESIA DEVICES - OTHER EUDAMED
GMDN Term
Medical gas flowmeter, Thorpe tube FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
868.2340 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Pulmonary function analysis system, adult

1mfa Series Flowmeters (oxygen by Precision Medical, Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary function analysis system, adult.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000008706
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 62c81fe6-a889-49cd-b985-200172c6ef73 61 fields · synced Jul 8, 2026
  • FDA UDI e317513d-4cea-42d4-9172-c9cf7c03be2a 34 fields · synced May 30, 2026