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 UDIBSB FDA UDI
- GMDN Term
- Conduction blood/fluid warmer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5725 FDA UDI864.9205 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
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
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Also classified as Conduction blood/fluid warmer.
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- EXPRESS FLUID WARMER — NxStage Medical, Inc. · Class II
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- QINFLOW AC STATION INTRO SET WARRIOR — QUALITY IN FLOW LTD · Class II
Cleared under the same submission
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Mequ A/S
Sources (1)
- FDA UDI c178c2a6-17ba-4291-887c-da30060698b9 36 fields · synced May 30, 2026