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MedSource Emergency Blanket

FDA UDI

Class I (US FDA UDI)

by Medsource International Llc

Identity

Trade Name
MedSource Emergency Blanket FDA UDI
Generic Name
Rescue blanket, reusable FDA UDI
Device Name
Blanket, Mylar, Emergency FDA UDI
Model / Reference
MS-B100-RCS FDA UDI
Description
Blanket, Mylar, Emergency FDA UDI

Identifiers

Catalog Number
Not Applicable FDA UDI
Primary DI / UDI-DI
00840155406131 FDA UDI
FDA Product Code
KME FDA UDI
GMDN Term
Rescue blanket, reusable 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: Rescue blanket, reusable

MedSource Emergency Blanket by Medsource International Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rescue blanket, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4b4ddec5-f0da-4ced-8d1f-f2fe056aa57e 34 fields · synced May 30, 2026