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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
Soft-tissue ultrasonic surgical system FDA UDI
Device Name
Electrode Electrosurgical Blade Extended Insulation Polytetrafluoroethylene Coated 2.5 Inch Sterile Not Made With Natural Rubber Latex MediChoice FDA UDI
Model / Reference
ES25021 FDA UDI
Description
Electrode Electrosurgical Blade Extended Insulation Polytetrafluoroethylene Coated 2.5 Inch Sterile Not Made With Natural Rubber Latex MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632110009 FDA UDI
510(k) Number
K081647 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Soft-tissue ultrasonic surgical system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Soft-tissue ultrasonic surgical system

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

Similar devices

Also classified as Soft-tissue ultrasonic surgical system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4f1b0eed-41a3-46fe-a23f-e40f6c3b6532 34 fields · synced May 31, 2026