MediChoice

FDA UDI

Class I (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name: MediChoice FDA UDI
Generic Name: Skin staple remover, single-use FDA UDI
Device Name: Tray Skin Staple Remover Scissor Style 3X3In Gauze Polyvinylpyrrolidone Preparation Pad Latex-Free Sterile MediChoice FDA UDI
Model / Reference: SSR1002 FDA UDI
Description: Tray Skin Staple Remover Scissor Style 3X3In Gauze Polyvinylpyrrolidone Preparation Pad Latex-Free Sterile MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI: 10885632126239 FDA UDI
FDA Product Code: KDD FDA UDI
GMDN Term: Skin staple remover, 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Skin staple remover, single-use

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Owens & Minor Distribution, Inc.

Sources (1)

FDA UDI f1b40afe-60b7-4236-b395-f84bf30b7787 34 fields · synced May 30, 2026