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Ventiseal Preformed Oral South(pos)et Tube Id 7.5 - Sterile
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- VENTISEAL PREFORMED ORAL SOUTH(POS)ET TUBE ID 7.5 - STERILE FDA UDI
- Generic Name
- Basic endotracheal tube, single-use FDA UDI
- Model / Reference
- 038-972-075U FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05055788727828 FDA UDI
- FDA Product Code
- BTR FDA UDI
- GMDN Term
- Basic endotracheal tube, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5730 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Basic endotracheal tube, single-use
Ventiseal Preformed Oral South(pos)et Tube Id 7.5 - Sterile by Flexicare Medical Limited — Class II — FDA UDI — listed in FDA GUDID
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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
- Flexicare Medical Limited
Sources (1)
- FDA UDI c055217b-874e-4244-8a01-88769de5c011 32 fields · synced May 29, 2026