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PM5200 Air/Oxygen Blender (High Flow)

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref Air/Oxygen Blender (High Flow)Model PM5200 SERIES,BLENDER,AIR/O2,HIGH FLOW

by Precision Medical Inc

Identity

Trade Name
PM5200 Air/Oxygen Blender (High Flow) EUDAMED
Precision Medical Blender FDA UDI
Generic Name
Oxygen/air breathing gas mixer, hospital FDA UDI
Device Name
PM5200 Series Blender EUDAMED
PM5200 SERIES,BLENDER,AIR/O2,HIGH FLOW FDA UDI
Model / Reference
PM5200 SERIES,BLENDER,AIR/O2,HIGH FLOW EUDAMED
Air/Oxygen Blender (High Flow) EUDAMED
PM5200 FDA UDI
Description
PM5200 SERIES,BLENDER,AIR/O2,HIGH FLOW FDA UDI

Identifiers

Primary DI / UDI-DI
00855887006009 EUDAMEDFDA UDI
Basic UDI-DI
B-00855887006009 EUDAMED
510(k) Number
K053232 FDA UDI
FDA Product Code
BZR FDA UDI
EMDN Code
R9099 RESPIRATORY AND ANAESTHESIA DEVICES - OTHER EUDAMED
GMDN Term
Oxygen/air breathing gas mixer, hospital FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
868.5330 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pulmonary function analysis system, adult

PM5200 Air/Oxygen Blender (High Flow) by Precision Medical, Inc. — Class IIb — 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 401eaf28-76aa-4b20-b0d0-c38dc6230132 61 fields · synced Oct 6, 2026
  • FDA UDI 31e6090e-452f-4c25-9824-181967dc8d2a 35 fields · synced May 30, 2026