← Back to catalogue

Oxygen Concentrator

FDA UDIEUDAMED

Class II (US FDA UDI)

by Sysmed (china) Co., Ltd

Identity

Trade Name
Oxygen Concentrator FDA UDI
Generic Name
Stationary oxygen concentrator FDA UDI
Model / Reference
M50 FDA UDI

Identifiers

Primary DI / UDI-DI
06955623000019 FDA UDI
510(k) Number
K172234 FDA UDI
FDA Product Code
CAW FDA UDI
GMDN Term
Stationary oxygen concentrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5440 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Stationary oxygen concentrator

Oxygen Concentrator by Sysmed (china) Co., Ltd — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Stationary oxygen concentrator.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA UDI c1659b72-3c48-453b-acf8-9f33cad725ab 33 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026