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Medi-First Emergency Survival Blanket

FDA UDI

Class I (US FDA UDI)

by Medique Products

Identity

Trade Name
Medi-First Emergency Survival Blanket FDA UDI
Generic Name
Bed linen set FDA UDI
Device Name
An emergency medical blanket intended for to be used by one patient for a period of time and then discarded. FDA UDI
Model / Reference
81001 FDA UDI
Description
An emergency medical blanket intended for to be used by one patient for a period of time and then discarded. FDA UDI

Identifiers

Catalog Number
81001 FDA UDI
Primary DI / UDI-DI
00347682810016 FDA UDI
FDA Product Code
KME FDA UDI
GMDN Term
Bed linen set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6060 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bed linen set

Medi-First Emergency Survival Blanket by Medique Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bed linen set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medique Products

Sources (1)

  • FDA UDI 7a3a7027-f4a2-4d65-8cb1-af608c206bf4 35 fields · synced May 30, 2026