FeatherTouch®

GUDID 20681490051532

RASP 1992210 FEATHERTOUCH 2PK FINE

MEDTRONIC XOMED, INC.

Nasal file/rasp

• Primary Device ID: 20681490051532
• NIH Device Record Key: 478b117d-05a0-4cd9-aa7c-acea3102f0ed
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FeatherTouch®
• Version Model Number: 1992210
• Company DUNS: 835465063
• Company Name: MEDTRONIC XOMED, INC.
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Width: 8 Millimeter
• Width: 8 Millimeter
• Width: 8 Millimeter
• Width: 8 Millimeter
• Width: 8 Millimeter
• Width: 8 Millimeter
• Width: 8 Millimeter
• Width: 8 Millimeter
• Width: 8 Millimeter
• Width: 8 Millimeter
• Width: 8 Millimeter
• Width: 8 Millimeter
• Width: 8 Millimeter
• Width: 8 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00681490051538 [Primary]
GS1	20681490051532 [Package]; Contains: 00681490051538; Package: PK [2 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K983025

FDA Product Code

• HRX: ARTHROSCOPE

Sterilization

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

[20681490051532]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490051532]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490051532]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490051532]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490051532]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490051532]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490051532]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490051532]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490051532]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490051532]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490051532]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490051532]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490051532]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490051532]

Moist Heat or Steam Sterilization;Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-12-07
• Device Publish Date: 2016-04-17

On-Brand Devices [FeatherTouch®]

• 20681490051532: RASP 1992210 FEATHERTOUCH 2PK FINE
• 20681490051525: RASP 1992208 FEATHERTOUCH 2PK COARSE
• 00681490051095: TRAY 1922006 FEATHERTOUCH STERILIZATION
• 00681490051088: CONVERTER 1922005 FEATHERTOUCH AUTO RASP
• 20681490049157: TUBING 1895524 10PK FEATHERTOUCH SUCTION