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therMaxTherMax Blood Warmer

FDA UDI

Class II (US FDA UDI)

by Baxter Healthcare Corp

Identity

Trade Name
therMaxTherMax Blood Warmer FDA UDI
Generic Name
Conduction blood/fluid warmer set FDA UDI
Device Name
The Blood Warmer Disposable is a disposable circuit for use with the TherMax blood warmer in combination with other PrisMax disposable sets. FDA UDI
Model / Reference
955516 FDA UDI
Description
The Blood Warmer Disposable is a disposable circuit for use with the TherMax blood warmer in combination with other PrisMax disposable sets. FDA UDI

Identifiers

Catalog Number
955516 FDA UDI
Primary DI / UDI-DI
07332414123932 FDA UDI
FDA Product Code
KDI FDA UDI
GMDN Term
Conduction blood/fluid warmer set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5860 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

Category: Conduction blood/fluid warmer set

therMaxTherMax Blood Warmer by Baxter Healthcare Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Conduction blood/fluid warmer set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 683ee3b2-ec4a-4b3a-8c46-cdb28e1348b6 35 fields · synced May 29, 2026