Identity
- Trade Name
- Venner™ Tracheal Seal Monitor Extension Tube FDA UDI
- Generic Name
- Medical air low pressure hose FDA UDI
- Device Name
- For facilitating the cuff inflation connection between the Venner™ Tracheal Seal Monitor and Venner™ PneuX P.Y.™ Endotracheal or Tracheostomy breathing tube. FDA UDI
- Model / Reference
- 903001 FDA UDI
- Description
- For facilitating the cuff inflation connection between the Venner™ Tracheal Seal Monitor and Venner™ PneuX P.Y.™ Endotracheal or Tracheostomy breathing tube. FDA UDI
Identifiers
- Catalog Number
- 903001 FDA UDI
- Primary DI / UDI-DI
- 08885009190851 FDA UDI
- FDA Product Code
- BYX FDA UDI
- GMDN Term
- Medical air low pressure hose FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5860 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Venner™ Tracheal Seal Monitor Extension Tube by Venner Medical (singapore) Pte. Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 0e8a0b9f-de54-454d-b951-e8291d48bfcd 35 fields · synced Jun 1, 2026