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Hypothermia Prevention Blanket

FDA UDI

Class I (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
Hypothermia Prevention Blanket FDA UDI
Generic Name
Hypothermia-prevention whole-body suit FDA UDI
Device Name
HYPOTHERMIA PREVENTION BLANKET 1 ea - 7.5' x 6.5' Blizzard Light Blanket FDA UDI
Model / Reference
00 FDA UDI
Description
HYPOTHERMIA PREVENTION BLANKET 1 ea - 7.5' x 6.5' Blizzard Light Blanket FDA UDI

Identifiers

Catalog Number
04-105 FDA UDI
Primary DI / UDI-DI
M689041050 FDA UDI
FDA Product Code
KME FDA UDI
IMD FDA UDI
GMDN Term
Hypothermia-prevention whole-body suit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6060 FDA UDI
890.5710 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Hypothermia Prevention Blanket by Safeguard Us Operating, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ecc38ca6-1674-44c5-8b2d-fd2c681f368e 35 fields · synced May 30, 2026