Identity
- Trade Name
- Coag Dissector FDA UDI
- Generic Name
- Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI
- Device Name
- The Coag Dissector is a monopolar electrosurgical instrument for dissection and hemostasis using flexible endoscopes • tip design inspired by laparoscopic surgical instruments • branches for blunt dissection of tissue • good coagulation capabilities between branches • rotatable flexible shaft for precise alignment of tip orientation • curved grasper for precise targeting of the tissue • teeth provide secure grasping of the bleeding area FDA UDI
- Model / Reference
- 165 cm FDA UDI
- Description
- The Coag Dissector is a monopolar electrosurgical instrument for dissection and hemostasis using flexible endoscopes • tip design inspired by laparoscopic surgical instruments • branches for blunt dissection of tissue • good coagulation capabilities between branches • rotatable flexible shaft for precise alignment of tip orientation • curved grasper for precise targeting of the tissue • teeth provide secure grasping of the bleeding area FDA UDI
Identifiers
- Catalog Number
- 200.50 FDA UDI
- Primary DI / UDI-DI
- 04260206311027 FDA UDI
- 510(k) Number
- K141794 FDA UDI
- FDA Product Code
- KGE 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
Category: Endoscopic electrosurgical handpiece/electrode, monopolar, single-use
Coag Dissector by Ovesco Endoscopy AG — 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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Cleared under the same submission
K141794 also covers:
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
- Ovesco Endoscopy AG
Sources (1)
- FDA UDI de561b9c-30e5-418c-9f76-a06abfaca509 38 fields · synced Jun 1, 2026