OTSC Anchor 220tt 200.11

GUDID 04260206310297

The OTSC Anchor 220tt is one of the OTSC application aids • can be used for treating a lesion before release of the OTSC clip • can be used for better approximation of tissue especially when indurated (e.g. fistulae, chronic ulcer) • facilitates targeting lesions, e.g. in the treatment of hemorrhage • allows precise alignment between the target tissue and the application cap • the head of the instrument is made of Nitinol • a working channel diameter of at least 3.2 mm is required when used in combination with the OTSC System

Ovesco Endoscopy AG

Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use

• Primary Device ID: 04260206310297
• NIH Device Record Key: 048dcc52-c325-4684-b23c-7ff3a0ede9dd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OTSC Anchor 220tt
• Version Model Number: 220 cm
• Catalog Number: 200.11
• Company DUNS: 344007369
• Company Name: Ovesco Endoscopy AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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
• Phone: +49707196528160
• Email: service@ovesco.com
• Phone: +49707196528160
• Email: service@ovesco.com
• Phone: +49707196528160
• Email: service@ovesco.com
• Phone: +49707196528160
• Email: service@ovesco.com
• Phone: +49707196528160
• Email: service@ovesco.com
• Phone: +49707196528160
• Email: service@ovesco.com
• Phone: +49707196528160
• Email: service@ovesco.com
• Phone: +49707196528160
• Email: service@ovesco.com
• Phone: +49707196528160
• Email: service@ovesco.com
• Phone: +49707196528160
• Email: service@ovesco.com
• Phone: +49707196528160
• Email: service@ovesco.com
• Phone: +49707196528160
• Email: service@ovesco.com
• Phone: +49707196528160
• Email: service@ovesco.com
• Phone: +49707196528160
• Email: service@ovesco.com

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Device Identifiers

Device Issuing Agency	Device ID
GS1	04260206310297 [Primary]

FDA Product Code

• KOA: Surgical Instruments, G-U, Manual (And Accessories)
• PTS: Endoscopic Grasping/Cutting Instrument, Non-Powered, Exempt

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-10-31
• Device Publish Date: 2016-09-16

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• 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