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°M Warmer System - Power Pack

FDA UDI

Class II (US FDA UDI)

by Mequ A/S

Identity

Trade Name
°M Warmer System - Power Pack FDA UDI
Generic Name
Conduction blood/fluid warmer FDA UDI
Device Name
Rechargeable battery pack for powering the °M Warmer FDA UDI
Model / Reference
MWS105 FDA UDI
Description
Rechargeable battery pack for powering the °M Warmer FDA UDI

Identifiers

Catalog Number
MWS105 FDA UDI
Primary DI / UDI-DI
05745000140039 FDA UDI
510(k) Number
K232107 FDA UDI
FDA Product Code
LGZ FDA UDI
BSB FDA UDI
GMDN Term
Conduction blood/fluid warmer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 FDA UDI
864.9205 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Conduction blood/fluid warmer

°M Warmer System - Power Pack by Mequ A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Conduction blood/fluid warmer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mequ A/S

Sources (1)

  • FDA UDI c178c2a6-17ba-4291-887c-da30060698b9 36 fields · synced May 30, 2026