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 used to endoscopically grasp, dissect, and transect tissue during Gastrointestinal (GI) endoscopic procedures. The snare can be used with or without the use of monopolar diathermic energy. FDA UDI
- Model / Reference
- 00711119 FDA UDI
- Description
- The Lariat snare is an electrosurgical device used to endoscopically grasp, dissect, and transect tissue during Gastrointestinal (GI) endoscopic procedures. The snare can be used with or without the use of monopolar diathermic energy. FDA UDI
Identifiers
- Catalog Number
- 00711119 FDA UDI
- Primary DI / UDI-DI
- 00724995182632 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
- 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
- Outer Diameter — 2 Millimeter FDA UDILength — 230 Centimeter FDA UDI
Category: Endoscopic electrosurgical handpiece/electrode, monopolar, single-use
Lariat by US Endoscopy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Endoscopic electrosurgical handpiece/electrode, monopolar, single-use.
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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 f7277f9c-07c0-4db2-a7a7-9c86396081bf 37 fields · synced May 30, 2026