Coag Endo-Dissector 200.50

GUDID 04260206310341

The Coag Endo-Dissector is a monopolar electrosurgical instrument for dissection and hemostasis using flexible endoscopes • branches for blunt dissection of tissue • good coagulation capabilities between branches • rotatable flexible shaft for precise alignment of tip • curved grasper for precise targeting of the tissue • teeth provide secure grasping of the bleeding area

Ovesco Endoscopy AG

Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use

• Primary Device ID: 04260206310341
• NIH Device Record Key: 49578c0d-3acc-4fff-97f2-5420dc88bab1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Coag Endo-Dissector
• Version Model Number: 165 cm
• Catalog Number: 200.50
• Company DUNS: 344007369
• Company Name: Ovesco Endoscopy AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +49707196528160
• Email: service@ovesco.com
• Phone: +49707196528160
• Email: service@ovesco.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Storage Environment Humidity: Between 15 Percent (%) Relative Humidity and 70 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 15 Percent (%) Relative Humidity and 70 Percent (%) Relative Humidity

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260206310341 [Previous]
GS1	04260206311027 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K141794

FDA Product Code

• KGE: Forceps, Biopsy, Electric

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-10-31
• Device Publish Date: 2016-09-16

Devices Manufactured by Ovesco Endoscopy AG

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• 04260206311379 - BougieCap: 2022-10-10 The BougieCap is for dilation of strictures in the upper gastrointestinal tract • the transparent cap allows direct visual c
• 04260206311393 - BougieCap: 2022-10-10 The BougieCap is for dilation of strictures in the upper gastrointestinal tract • the transparent cap allows direct visual c
• 04260206311416 - BougieCap: 2022-10-10 The BougieCap is for dilation of strictures in the upper gastrointestinal tract • the transparent cap allows direct visual c
• 04260206311430 - BougieCap: 2022-10-10 The BougieCap is for dilation of strictures in the upper gastrointestinal tract • the transparent cap allows direct visual c
• 04260206311454 - BougieCap: 2022-10-10 The BougieCap is for dilation of strictures in the upper gastrointestinal tract • the transparent cap allows direct visual c
• 04260206311478 - BougieCap: 2022-10-10 The BougieCap is for dilation of strictures in the upper gastrointestinal tract • the transparent cap allows direct visual c