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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
Endoscope antifog solution FDA UDI
Device Name
Solution Endoscopic Anti-Fog Non-Toxic Non-Abrasive 6 Cubic Centimeter With Radiopaque Adhesive-Backed Sponge Sterile Not Made With Natural Rubber Latex MediChoice FDA UDI
Model / Reference
FOG1001 FDA UDI
Description
Solution Endoscopic Anti-Fog Non-Toxic Non-Abrasive 6 Cubic Centimeter With Radiopaque Adhesive-Backed Sponge Sterile Not Made With Natural Rubber Latex MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632110696 FDA UDI
510(k) Number
K932449 FDA UDI
FDA Product Code
OCT FDA UDI
GMDN Term
Endoscope antifog solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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: Endoscope antifog solution

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

Similar devices

Also classified as Endoscope antifog solution.

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 2fac1ab8-6c52-4ac2-b24c-5eeba059ca89 34 fields · synced May 30, 2026