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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
Tube/mask breathing circuit connector, single-use, sterile FDA UDI
Device Name
Tubing Suction 2 Connector Non-Conductive Heavy-Duty Durable Flexible With Male Adapter Polyvinyl Chloride 12 Feet X 0.1875 Inch Sterile Not Made With Natural Rubber Latex MediChoice FDA UDI
Model / Reference
ST1003 FDA UDI
Description
Tubing Suction 2 Connector Non-Conductive Heavy-Duty Durable Flexible With Male Adapter Polyvinyl Chloride 12 Feet X 0.1875 Inch Sterile Not Made With Natural Rubber Latex MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632100987 FDA UDI
FDA Product Code
BYY FDA UDI
GMDN Term
Tube/mask breathing circuit connector, single-use, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

No

FDA UDI

Category: Tube/mask breathing circuit connector, single-use, sterile

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

Similar devices

Also classified as Tube/mask breathing circuit connector, single-use, sterile.

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 4235da00-ec7a-4e5b-8358-8fd2e7256c19 34 fields · synced May 30, 2026