← Back to catalogue

MediChoice

FDA UDI

Class I (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name
MediChoice FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Rigid Container Sterilization 11.5x11x5 Stainless Steel Silver CA/1 Not made with Natural Rubber Latex Medichoice FDA UDI
Model / Reference
58239 FDA UDI
Description
Rigid Container Sterilization 11.5x11x5 Stainless Steel Silver CA/1 Not made with Natural Rubber Latex Medichoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632436451 FDA UDI
510(k) Number
K131407 FDA UDI
K233578 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Instrument tray, reusable 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Instrument tray, reusable

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

Similar devices

Also classified as Instrument tray, reusable.

Cleared under the same submission

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 047610a5-34c4-44c5-a2bf-7e3393c666de 34 fields · synced May 30, 2026