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FilteredFlo® Cardiac Blanket

FDA UDI

Class II (US FDA UDI)

by Gentherm Medical, LLC

Identity

Trade Name
FilteredFlo® Cardiac Blanket FDA UDI
Generic Name
Circulating-air whole-body heating/cooling system pad, single-use, sterile FDA UDI
Device Name
Thermal Regulating System FDA UDI
Model / Reference
542 FDA UDI
Description
Thermal Regulating System FDA UDI

Identifiers

Catalog Number
82542 FDA UDI
Primary DI / UDI-DI
20613031825425 FDA UDI
FDA Product Code
DWJ FDA UDI
GMDN Term
Circulating-air whole-body heating/cooling system pad, single-use, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 50.0 Inch FDA UDI
Length — 72.0 Inch FDA UDI
Weight — 0.7 Pound FDA UDI

Category: Circulating-air whole-body heating/cooling system pad, single-use, sterile

FilteredFlo® Cardiac Blanket by Gentherm Medical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Circulating-air whole-body heating/cooling system pad, single-use, sterile.

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 31937451-9203-4609-8f07-072c9208bef8 37 fields · synced May 31, 2026