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Action®

FDA UDI

Class I (US FDA UDI)

by Action Products, Inc.

Identity

Trade Name
Action® FDA UDI
Generic Name
Operating table patient pressure distribution pad, reusable FDA UDI
Device Name
Isolette Pad FDA UDI
Model / Reference
Overlay FDA UDI
Description
Isolette Pad FDA UDI

Identifiers

Catalog Number
40120L FDA UDI
Primary DI / UDI-DI
00089904000583 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Operating table patient pressure distribution pad, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6450 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Operating table patient pressure distribution pad, reusable

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

Similar devices

Also classified as Operating table patient pressure distribution pad, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Action Products, Inc.

Sources (1)

  • FDA UDI 47b61017-fed5-460f-94c0-6b9bc8b9dc00 36 fields · synced Jun 9, 2026