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Medical Action Industries

FDA UDI

Class II (US FDA UDI)

by Medical Action Industries Inc.

Identity

Trade Name
Medical Action Industries FDA UDI
Generic Name
Dry medical towel/wipe, single-use FDA UDI
Device Name
Towel: OR Grn XR Pret 400/cs FDA UDI
Model / Reference
731-G4X FDA UDI
Description
Towel: OR Grn XR Pret 400/cs FDA UDI

Identifiers

Primary DI / UDI-DI
10809160002438 FDA UDI
FDA Product Code
KKX FDA UDI
GMDN Term
Dry medical towel/wipe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dry medical towel/wipe, single-use

Medical Action Industries by Medical Action Industries Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dry medical towel/wipe, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dd913134-8ea5-48c6-a28a-c51c3e6a2e87 33 fields · synced May 30, 2026