Air/Water Bottle CO2 Tubing

FDA UDI

Class II (US FDA UDI)

by Micro-tech Usa

Identity

Trade Name: Air/Water Bottle CO2 Tubing FDA UDI
Generic Name: Endoscopic insufflation tubing set, single-use FDA UDI
Device Name: Air/Water Bottle CO2 Tubing Olympus FDA UDI
Model / Reference: AW02-OLYC02 FDA UDI
Description: Air/Water Bottle CO2 Tubing Olympus FDA UDI

Identifiers

Primary DI / UDI-DI: 00850025860390 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

Air/Water Bottle CO2 Tubing by Micro-tech Usa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic insufflation tubing set, single-use.

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Olympus — Keymed (Medical & Industrial Equipment), Ltd. · Class II
ERBEFLO CleverCap® — Erbe Medical, LLC · Class II
ENDO SMARTCAP — MEDIVATORS INC. · Class II
ENDO SMARTCAP — MEDIVATORS INC. · Class II
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 34491496-5511-4bbb-9821-0e92ddcb4902 33 fields · synced Jun 1, 2026