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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
Suction system catheter, general-purpose FDA UDI
Device Name
Catheter Suction Delee Tip Straight 10 French 16 Inch Pediatric With Control Vent Polyvinyl Chloride Sterile Not Made With Natural Rubber Latex MediChoice FDA UDI
Model / Reference
RSC10D FDA UDI
Description
Catheter Suction Delee Tip Straight 10 French 16 Inch Pediatric With Control Vent Polyvinyl Chloride Sterile Not Made With Natural Rubber Latex MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632100727 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Suction system catheter, general-purpose 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: Suction system catheter, general-purpose

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

Similar devices

Also classified as Suction system catheter, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 68f4b8fe-11b9-45af-a3cc-a3b4249b419f 34 fields · synced May 31, 2026