← Back to catalogue

Allcare

FDA UDI

Class I (US FDA UDI)

by Allcare, Inc.

Identity

Trade Name
ALLCARE FDA UDI
Generic Name
Bed blanket, single-use FDA UDI
Device Name
FLEECE BLANKET, HEAVYWEIGHT, MAROON, 60" X 90", 10/Case FDA UDI
Model / Reference
EB500M FDA UDI
Description
FLEECE BLANKET, HEAVYWEIGHT, MAROON, 60" X 90", 10/Case FDA UDI

Identifiers

Primary DI / UDI-DI
10182921000622 FDA UDI
FDA Product Code
KME FDA UDI
GMDN Term
Bed blanket, single-use 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

Yes

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

Yes

FDA UDI

Category: Bed blanket, single-use

Allcare by Allcare, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bed blanket, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Allcare, Inc.

Sources (1)

  • FDA UDI 98db5a6c-059a-4dc0-8e63-785729900dc5 35 fields · synced May 30, 2026