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AllCare

FDA UDI

Class I (US FDA UDI)

by Allcare, Inc.

Identity

Trade Name
AllCare FDA UDI
Generic Name
Basic pillowcase, reusable FDA UDI
Device Name
UNIVERSAL PILLOW CASE, 21" x 30", WHITE FDA UDI
Model / Reference
PL100 FDA UDI
Description
UNIVERSAL PILLOW CASE, 21" x 30", WHITE FDA UDI

Identifiers

Catalog Number
PL100 FDA UDI
Primary DI / UDI-DI
00182921000496 FDA UDI
FDA Product Code
KME FDA UDI
GMDN Term
Basic pillowcase, 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: Basic pillowcase, reusable

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

Similar devices

Also classified as Basic pillowcase, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Allcare, Inc.

Sources (1)

  • FDA UDI d13dc585-8aab-43f7-8628-2c06ed6b7fe9 36 fields · synced May 30, 2026