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Maxi-Therm®

FDA UDI

Class II (US FDA UDI)

by Gentherm Medical, LLC

Identity

Trade Name
Maxi-Therm® FDA UDI
Generic Name
External circulating-fluid core temperature regulation system pad, single-use FDA UDI
Device Name
Hyper-Hypothermia Blanket FDA UDI
Model / Reference
273 FDA UDI
Description
Hyper-Hypothermia Blanket FDA UDI

Identifiers

Catalog Number
82273 FDA UDI
Primary DI / UDI-DI
20613031822738 FDA UDI
FDA Product Code
ILO FDA UDI
GMDN Term
External circulating-fluid core temperature regulation system pad, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5720 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 30.5 Centimeter FDA UDI
Length — 45.7 Centimeter FDA UDI
Width — 12 Inch FDA UDI
Length — 18 Inch FDA UDI
Weight — 0.33 Pound FDA UDI

Category: External circulating-fluid core temperature regulation system pad, single-use

Maxi-Therm® by Gentherm Medical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External circulating-fluid core temperature regulation system pad, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gentherm Medical, LLC

Sources (1)

  • FDA UDI a8bb387f-1679-4fe0-b38d-7f412f218f92 37 fields · synced Jun 1, 2026