← Back to catalogue

MediChoice

FDA UDI

Class I (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name
MediChoice FDA UDI
Generic Name
General-purpose surgical scissors, single-use FDA UDI
Device Name
Scissor Operating Room Straight Blunt/Sharp Stainless Steel 5.5 Inch Not Made With Natural Rubber Latex Sterile MediChoice FDA UDI
Model / Reference
FG6001 FDA UDI
Description
Scissor Operating Room Straight Blunt/Sharp Stainless Steel 5.5 Inch Not Made With Natural Rubber Latex Sterile MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632110566 FDA UDI
FDA Product Code
KDC FDA UDI
GMDN Term
General-purpose surgical scissors, 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: General-purpose surgical scissors, 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 General-purpose surgical scissors, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 12e28562-99da-41c1-9344-8a4d9634d6d2 34 fields · synced Jun 6, 2026