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MediChoice

FDA UDI

Class I (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name
MediChoice FDA UDI
Generic Name
Suture removal kit FDA UDI
Device Name
Tray Suture Removal 3X3In Gauze Iris Scissor Straight 4.5In Adson Forcep Serrated 4.75In Large Alcohol Preparation Pad Polyvinylpyrrolidone Latex-Free Sterile MediChoice FDA UDI
Model / Reference
SUT1004 FDA UDI
Description
Tray Suture Removal 3X3In Gauze Iris Scissor Straight 4.5In Adson Forcep Serrated 4.75In Large Alcohol Preparation Pad Polyvinylpyrrolidone Latex-Free Sterile MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632126895 FDA UDI
FDA Product Code
MCZ FDA UDI
GMDN Term
Suture removal kit 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suture removal kit

MediChoice by Owens & Minor Distribution, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suture removal kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a6ed6a4f-ed0a-418f-8959-bb99c8d55771 34 fields · synced Jun 8, 2026