Identity
- Trade Name
- LOADING CONE FDA UDI
- Generic Name
- Haemorrhoid ligator FDA UDI
- Device Name
- LOADING CONE FDA UDI
- Model / Reference
- 508-570 FDA UDI
- Description
- LOADING CONE FDA UDI
Identifiers
- Catalog Number
- 508-570 FDA UDI
- Primary DI / UDI-DI
- 00192896096080 FDA UDI
- FDA Product Code
- FHN FDA UDI
- GMDN Term
- Haemorrhoid ligator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.4400 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 12 Millimeter FDA UDI
Category: Haemorrhoid ligator
Loading Cone by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Haemorrhoid ligator.
- V. Mueller — STERIS CORPORATION · Class II
- Novo Surgical — NOVO SURGICAL, INC. · Class II
- Sklar® — Sklar Corporation · Class I
- Avalign — AVALIGN TECHNOLOGIES, Inc. · Class II
- ESI — FTT MEDICAL, INC. · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
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
- Sontec Instruments, Inc.
Sources (1)
- FDA UDI 3ed74376-1e32-4a8f-8311-4c7580d4849e 36 fields · synced May 30, 2026