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Bair Hugger™

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name
Bair Hugger™ FDA UDI
Generic Name
External circulating-air core temperature regulation system pad, single-use FDA UDI
Device Name
3M™ Bair Hugger™ Pediatric Underbody Blanket, 10 per case, 55501 FDA UDI
Model / Reference
55501 FDA UDI
Description
3M™ Bair Hugger™ Pediatric Underbody Blanket, 10 per case, 55501 FDA UDI

Identifiers

Catalog Number
55501 FDA UDI
Primary DI / UDI-DI
50707387775051 FDA UDI
510(k) Number
K060865 FDA UDI
FDA Product Code
DWJ FDA UDI
GMDN Term
External circulating-air core temperature regulation system pad, single-use 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

Bair Hugger™ by 3m Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 6de49070-eb1a-4d9d-8aa8-9a4fa38ea0c6 36 fields · synced May 30, 2026