← Back to catalogue

Allcare

FDA UDI

Class I (US FDA UDI)

by Allcare, Inc.

Identity

Trade Name
ALLCARE FDA UDI
Generic Name
Bed linen set FDA UDI
Device Name
EMS Linen Pack; EF600 Stretcher sheet, FS200 Patient Sheet, PL100 Pillowcase FDA UDI
Model / Reference
CK613 FDA UDI
Description
EMS Linen Pack; EF600 Stretcher sheet, FS200 Patient Sheet, PL100 Pillowcase FDA UDI

Identifiers

Catalog Number
CK613 FDA UDI
Primary DI / UDI-DI
00182921000670 FDA UDI
FDA Product Code
KME FDA UDI
GMDN Term
Bed linen set 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

Yes

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 linen set

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

Similar devices

Also classified as Bed linen set.

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 9fd01873-8571-4a5c-b459-fdab98ae8cba 36 fields · synced Jun 6, 2026