Identity
- Trade Name
- TEXAS FDA UDI
- Generic Name
- Basic endotracheal tube, reusable FDA UDI
- Device Name
- TRACHEAL SCOPE-TUBE ID 15MM OD 17mm, TL 337mm, for use with the optical element 82510.1400 and head systems 825101100 and 825101200, without distal viewing window, graduated, reusable FDA UDI
- Model / Reference
- 825211230 FDA UDI
- Description
- TRACHEAL SCOPE-TUBE ID 15MM OD 17mm, TL 337mm, for use with the optical element 82510.1400 and head systems 825101100 and 825101200, without distal viewing window, graduated, reusable FDA UDI
Identifiers
- Catalog Number
- 825211230 FDA UDI
- Primary DI / UDI-DI
- 04055207056769 FDA UDI
- FDA Product Code
- KTI FDA UDI
- GMDN Term
- Basic endotracheal tube, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.4680 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Lumen/Inner Diameter — 15 Millimeter FDA UDI
Texas by Richard Wolf GmbH — Class II — 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Richard Wolf GmbH
Sources (1)
- FDA UDI 5926f152-a807-493b-8905-41318f2185d5 37 fields · synced Jun 8, 2026