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Barrier® EasyWarm®

FDA UDI

Class II (US FDA UDI)

by Mölnlycke Health Care AB

Identity

Trade Name
Barrier® EasyWarm® FDA UDI
Generic Name
Activated-medium surgical warming blanket FDA UDI
Device Name
EasyWarm, ACTIVE SELF-WARMING BLANKET, 92x152 cm FDA UDI
Model / Reference
629905 FDA UDI
Description
EasyWarm, ACTIVE SELF-WARMING BLANKET, 92x152 cm FDA UDI

Identifiers

Primary DI / UDI-DI
07333350371685 FDA UDI
510(k) Number
K232508 FDA UDI
FDA Product Code
DWJ FDA UDI
GMDN Term
Activated-medium surgical warming blanket 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

No

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Activated-medium surgical warming blanket

Barrier® EasyWarm® by Mölnlycke Health Care AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Activated-medium surgical warming blanket.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 607cf11a-5d2f-4e97-817b-4032a2f5b521 36 fields · synced Jun 8, 2026