Emergency Blanket

by Medsource Factory, Inc. 16 variants

Ref 316650

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number697529369280118P Basic UDI-DI	Date6 Jan 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference: 316650

Primary DI / UDI-DI: 06975293690006
Basic UDI-DI: 697529369280118P
EMDN Code: V9099 Various devices not included in other classes - other

Device Class: Class I
Market of Registration: Germany

Manufacturer details

EUDAMED SRN: CN-MF-000047853
Authorised representative: MedPath GmbH DE-AR-000000087

Other devices from Medsource Factory, Inc.

Medical Disposable Isolation Gown

Class I
Medical Disposable Pants

Class I
Tourniquet

Class I
Patient Transfer Sheet

Class I
Splints

Class I
Emergency Blanket

Class I

See all devices from Medsource Factory, Inc. →

Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No