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Sure Care

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Sure Care FDA UDI
Generic Name
Cottonoid pad FDA UDI
Device Name
Fluff and Polymer Underpad,Heavy FDA UDI
Model / Reference
1552MD FDA UDI
Description
Fluff and Polymer Underpad,Heavy FDA UDI

Identifiers

Catalog Number
1552MD FDA UDI
Primary DI / UDI-DI
20884527001511 FDA UDI
FDA Product Code
KME FDA UDI
GMDN Term
Cottonoid pad 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

No

FDA UDI

Dimensions & Sizes

Size
Width — 30 Inch FDA UDI
Length — 36 Inch FDA UDI

Category: Cottonoid pad

Sure Care by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cottonoid pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 22833f70-055c-4c04-a7f4-971321d17def 37 fields · synced Jun 6, 2026