MediChoice

FDA UDI

Class I (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name: MediChoice FDA UDI
Generic Name: Endoscopic insufflation tubing set, single-use FDA UDI
Device Name: Tubing Insufflation 0.1 Micron Filter Luer Funnel Connect Stryker DEHP-Free Polyvinyl Chloride 10 Feet Sterile Not Made With Natural Rubber Latex MediChoice FDA UDI
Model / Reference: INSF1003 FDA UDI
Description: Tubing Insufflation 0.1 Micron Filter Luer Funnel Connect Stryker DEHP-Free Polyvinyl Chloride 10 Feet Sterile Not Made With Natural Rubber Latex MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI: 10885632112935 FDA UDI
FDA Product Code: NKC FDA UDI
GMDN Term: Endoscopic insufflation tubing set, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 884.1730 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic insufflation tubing set, single-use

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

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ENDO SMARTCAP — MEDIVATORS INC. · Class II
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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Owens & Minor Distribution, Inc.

Sources (1)

FDA UDI 11e448f5-9812-486c-b7ea-6993bbcde5d6 33 fields · synced May 31, 2026