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Medichoice

FDA UDI

Class II (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name
Medichoice FDA UDI
Generic Name
Electrosurgical/ultrasonic surgical system tester interface FDA UDI
Device Name
Combo No FDA Class II Kit No MFG Date MRI Unsafe Medical Device-Tax Non Sterile Not Nat Rubber Ltx Prescription Use RX Reusable FDA UDI
Model / Reference
CL8222 FDA UDI
Description
Combo No FDA Class II Kit No MFG Date MRI Unsafe Medical Device-Tax Non Sterile Not Nat Rubber Ltx Prescription Use RX Reusable FDA UDI

Identifiers

Primary DI / UDI-DI
10885632146688 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Electrosurgical/ultrasonic surgical system tester interface FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2900 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Electrosurgical/ultrasonic surgical system tester interface

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

Similar devices

Also classified as Electrosurgical/ultrasonic surgical system tester interface.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Owens & Minor Distribution, Inc.

Sources (1)

  • FDA UDI 9199ef53-d79a-4753-b73a-7881c49419a4 34 fields · synced Jun 8, 2026