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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
Suture kit, non-medicated FDA UDI
Device Name
Kit: Laceration 20/Cs FDA UDI
Model / Reference
68720 FDA UDI
Description
Kit: Laceration 20/Cs FDA UDI

Identifiers

Primary DI / UDI-DI
10809160022955 FDA UDI
FDA Product Code
OVN FDA UDI
GMDN Term
Suture kit, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4830 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suture kit, non-medicated

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 Suture kit, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Action Industries Inc.

Sources (1)

  • FDA UDI fd162064-6f00-4d66-9cd8-fc44057ea976 34 fields · synced May 30, 2026