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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
Operative-site suture holder FDA UDI
Device Name
Suture Guide Curved 8 Numbered A And B Slots Single Patient Use, Sterile White Hdpe Base, Blue Pvc Insert, White Foam Tape With High Tack Adhesive, White Paper Liner 3 Per Pack MediChoice FDA UDI
Model / Reference
SG0001 FDA UDI
Description
Suture Guide Curved 8 Numbered A And B Slots Single Patient Use, Sterile White Hdpe Base, Blue Pvc Insert, White Foam Tape With High Tack Adhesive, White Paper Liner 3 Per Pack MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
20885632065412 FDA UDI
FDA Product Code
GEJ FDA UDI
GMDN Term
Operative-site suture holder 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

Yes

FDA UDI

Category: Operative-site suture holder

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

Similar devices

Also classified as Operative-site suture holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b4683ed6-898b-4ec5-96d9-e13d6517ccc7 33 fields · synced May 30, 2026