← Back to catalogue

AllCare, INC

FDA UDI

Class I (US FDA UDI)

by Allcare, Inc.

Identity

Trade Name
AllCare, INC FDA UDI
Generic Name
Bed pillow, reusable FDA UDI
Device Name
SMALL PILLOW, BLUE, 14" X 16", DISPOSABLE FDA UDI
Model / Reference
PL200 FDA UDI
Description
SMALL PILLOW, BLUE, 14" X 16", DISPOSABLE FDA UDI

Identifiers

Catalog Number
PL200 FDA UDI
Primary DI / UDI-DI
00182921000533 FDA UDI
FDA Product Code
KME FDA UDI
GMDN Term
Bed pillow, 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

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 pillow, reusable

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

Similar devices

Also classified as Bed pillow, reusable.

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 363c2c2e-8a5a-44c9-8bae-8929c17bebca 36 fields · synced May 30, 2026