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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
Scalpel, single-use FDA UDI
Device Name
Scalpel Surgical Safety Fixed Blade With Movable Sheath Stainless Steel Size 11 Disposable Sterile Not Made With Natural Rubber Latex MediChoice FDA UDI
Model / Reference
55611 FDA UDI
Description
Scalpel Surgical Safety Fixed Blade With Movable Sheath Stainless Steel Size 11 Disposable Sterile Not Made With Natural Rubber Latex MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632104817 FDA UDI
FDA Product Code
GDX FDA UDI
GMDN Term
Scalpel, 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

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: Scalpel, single-use

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

Similar devices

Also classified as Scalpel, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d6e8e65c-c4c8-48c3-8a9f-2e6ff5fa57cf 33 fields · synced May 30, 2026