Identity
- Trade Name
- Lariat FDA UDI
- Generic Name
- Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI
- Device Name
- The Lariat snare is an electrosurgical device designed to be used to endoscopically grasp, dissect, and transect tissue during Gastrointestinal (GI) endoscopic procedures. FDA UDI
- Model / Reference
- 00711096 FDA UDI
- Description
- The Lariat snare is an electrosurgical device designed to be used to endoscopically grasp, dissect, and transect tissue during Gastrointestinal (GI) endoscopic procedures. FDA UDI
Identifiers
- Catalog Number
- 00711096 FDA UDI
- Primary DI / UDI-DI
- 00816765015230 FDA UDI
- 510(k) Number
- K151197 FDA UDI
- FDA Product Code
- FDI FDA UDI
- GMDN Term
- Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.4300 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
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 230 Centimeter FDA UDIOuter Diameter — 2 Millimeter FDA UDI
Lariat by US Endoscopy — 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
- US Endoscopy
Sources (1)
- FDA UDI 685b5b45-2695-49e6-ac40-39aa94bd8199 39 fields · synced Jun 8, 2026