Venner PneuX TSM™ Extension Tube(non-sterile)

FDA UDI

Class I (US FDA UDI)

by Venner Medical (singapore) Pte. Ltd.

Identity

Trade Name: Venner PneuX TSM™ Extension Tube(non-sterile) FDA UDI
Generic Name: Artificial airway cuff inflation tubing FDA UDI
Device Name: For facilitating the cuff inflation connection between the Venner PneuX TSM™ and an Venner PneuX™ Endotracheal or Tracheostomy breathing tube. FDA UDI
Model / Reference: 903010 FDA UDI
Description: For facilitating the cuff inflation connection between the Venner PneuX TSM™ and an Venner PneuX™ Endotracheal or Tracheostomy breathing tube. FDA UDI

Identifiers

Catalog Number: 903010 FDA UDI
Primary DI / UDI-DI: 08885009190905 FDA UDI
FDA Product Code: BYX FDA UDI
GMDN Term: Artificial airway cuff inflation tubing FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5860 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Artificial airway cuff inflation tubing

Venner PneuX TSM™ Extension Tube(non-sterile) by Venner Medical (singapore) Pte. Ltd. — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Venner Medical (singapore) Pte. Ltd.

Sources (1)

FDA UDI 30820246-8a29-4228-ab0e-66e5c50823da 34 fields · synced May 30, 2026