Identity
- Trade Name
- Davol Tracheal Suction Catheter FDA UDI
- Generic Name
- Airway suction catheter FDA UDI
- Device Name
- Davol Suction Catheter with funnel end, two eyes, whistle tip X-Ray Oraque Rubber FDA UDI
- Model / Reference
- 0108100 FDA UDI
- Description
- Davol Suction Catheter with funnel end, two eyes, whistle tip X-Ray Oraque Rubber FDA UDI
Identifiers
- Catalog Number
- 0108100 FDA UDI
- Primary DI / UDI-DI
- 00801741050510 FDA UDI
- FDA Product Code
- BSY FDA UDI
- GMDN Term
- Airway suction catheter FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.6810 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
Yes
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Davol Tracheal Suction Catheter by C. R. Bard, Inc. — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- C. R. Bard, Inc.
Sources (1)
- FDA UDI bb9bdd09-83fb-41ef-b656-d8d1903ccb19 37 fields · synced May 31, 2026