Heated High-Flow Tube Set

FDA UDI

Class II (US FDA UDI)

by W.O.M. World of Medicine GmbH

Identity

Trade Name: HEATED HIGH-FLOW TUBE SET FDA UDI
Generic Name: Endoscopic insufflation tubing set, single-use FDA UDI
Model / Reference: 0620050200 FDA UDI

Identifiers

Primary DI / UDI-DI: 04056702001568 FDA UDI
FDA Product Code: OSV FDA UDI
HIF FDA UDI
GMDN Term: Endoscopic insufflation tubing set, single-use FDA UDI

Classification

Device Class: Class II 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

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

Heated High-Flow Tube Set by W.O.M. World of Medicine GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 II	Pending data

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Manufacturer

Manufacturer: W.O.M. World of Medicine GmbH

Sources (1)

FDA UDI 6f812f03-741b-453e-8216-fe986e082ed9 32 fields · synced May 30, 2026