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Cardinal Health

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
Hot/cold therapy pack, single-use FDA UDI
Device Name
Infant Transport Mattress Disc Activation 19 x 9.25 in. (48.2 x 23.4 cm) FDA UDI
Model / Reference
11475-010B FDA UDI
Description
Infant Transport Mattress Disc Activation 19 x 9.25 in. (48.2 x 23.4 cm) FDA UDI

Identifiers

Catalog Number
11475-010B FDA UDI
Primary DI / UDI-DI
00192253061256 FDA UDI
FDA Product Code
IMD FDA UDI
GMDN Term
Hot/cold therapy pack, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5710 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hot/cold therapy pack, single-use

Cardinal Health by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hot/cold therapy pack, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7383c368-e7a6-4c7d-8bc6-e3623a29c0e3 34 fields · synced Jun 8, 2026