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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
Sputum specimen container IVD FDA UDI
Device Name
Trap Specimen Mucous Vacuum Breaker With 10 French Catheter 20 Cubic Centimeter Polyurethane Sterile Not Made With Natural Rubber Latex MediChoice FDA UDI
Model / Reference
MST2010 FDA UDI
Description
Trap Specimen Mucous Vacuum Breaker With 10 French Catheter 20 Cubic Centimeter Polyurethane Sterile Not Made With Natural Rubber Latex MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632120343 FDA UDI
FDA Product Code
BYZ FDA UDI
GMDN Term
Sputum specimen container IVD 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: Sputum specimen container IVD

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

Similar devices

Also classified as Sputum specimen container IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f9159a16-d99e-410e-8aae-55075d7cbae3 34 fields · synced Jun 8, 2026