CO2 Source Tubing Filter Adapter Olympus

FDA UDI

Class II (US FDA UDI)

by Micro-tech Usa

Identity

Trade Name: CO2 Source Tubing Filter Adapter Olympus FDA UDI
Generic Name: Endoscopic insufflation tubing set, single-use FDA UDI
Device Name: CO2 Source Tubing Filter Adapter Olympus, Sterile, Single Day Use. FDA UDI
Model / Reference: BW02-CO2TUBAOLY FDA UDI
Description: CO2 Source Tubing Filter Adapter Olympus, Sterile, Single Day Use. FDA UDI

Identifiers

Primary DI / UDI-DI: 00850025860901 FDA UDI
FDA Product Code: OCX FDA UDI
GMDN Term: Endoscopic insufflation tubing set, single-use 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

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

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

CO2 Source Tubing Filter Adapter Olympus by Micro-tech Usa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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MediChoice — OWENS & MINOR DISTRIBUTION, INC. · Class I

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 II	Pending data

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Manufacturer

Manufacturer: Micro-tech Usa

Sources (1)

FDA UDI e01ba0b0-9cdb-45ba-bb7b-627f98c60113 33 fields · synced May 31, 2026