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Medical Action Industries

FDA UDI

Class I (US FDA UDI)

by Medical Action Industries Inc.

Identity

Trade Name
Medical Action Industries FDA UDI
Generic Name
Surgical instrument interim-placement holder, single-use FDA UDI
Device Name
Suture Bag:Moisture Resistent 100 Cs FDA UDI
Model / Reference
8300 FDA UDI
Description
Suture Bag:Moisture Resistent 100 Cs FDA UDI

Identifiers

Primary DI / UDI-DI
10809160023839 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Surgical instrument interim-placement holder, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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: Surgical instrument interim-placement holder, single-use

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

Similar devices

Also classified as Surgical instrument interim-placement holder, single-use.

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 e8441054-a1f5-48b8-9f4b-c538fd071d11 34 fields · synced Jun 1, 2026