Identity
- Trade Name
- Hydro-Surg FDA UDI
- Generic Name
- Surgical irrigation/aspiration cannula, non-illuminating, reusable FDA UDI
- Device Name
- Quick-Disconnect Endo-Pool Suction Cannula Probe Tip Size: 10mm/33cm FDA UDI
- Model / Reference
- 5105950 FDA UDI
- Description
- Quick-Disconnect Endo-Pool Suction Cannula Probe Tip Size: 10mm/33cm FDA UDI
Identifiers
- Catalog Number
- 5105950 FDA UDI
- Primary DI / UDI-DI
- 00801741077036 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Surgical irrigation/aspiration cannula, non-illuminating, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 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
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 33 Centimeter FDA UDIOuter Diameter — 10 Millimeter FDA UDI
Hydro-Surg by Davol Inc. — 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 |
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Manufacturer
- Manufacturer
- Davol Inc.
Sources (1)
- FDA UDI 8765334c-ee44-4b44-83db-2fe781eacb86 37 fields · synced Jun 6, 2026