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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
Haemostatic forceps FDA UDI
Device Name
Inst: Hemostat Kelly Wire 5.5in 20/Bx FDA UDI
Model / Reference
56221 FDA UDI
Description
Inst: Hemostat Kelly Wire 5.5in 20/Bx FDA UDI

Identifiers

Primary DI / UDI-DI
10809160003428 FDA UDI
FDA Product Code
KDC FDA UDI
GMDN Term
Haemostatic forceps 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: Haemostatic forceps

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 Haemostatic forceps.

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 007aca29-4d46-457f-85de-e77b44bf21c0 34 fields · synced May 30, 2026