MPS®

GUDID 20681490073817

HANDPIECE 3327700 POWERFORMA STRAIGHT

MEDTRONIC XOMED, INC.

Multi-purpose surgical power tool system, line-powered

• Primary Device ID: 20681490073817
• NIH Device Record Key: 41ecb378-1423-47b2-b1f1-9217d6e17ffa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MPS®
• Version Model Number: 3327700
• 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: false
• Serial Number: true
• 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
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	20681490073817 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K960853

FDA Product Code

• ERL: DRILL, SURGICAL, ENT (ELECTRIC OR PNEUMATIC) INCLUDING HANDPIECE

Sterilization

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

[20681490073817]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490073817]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490073817]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490073817]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490073817]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490073817]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490073817]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490073817]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490073817]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490073817]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490073817]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490073817]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490073817]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490073817]

Moist Heat or Steam Sterilization;Ethylene Oxide

[20681490073817]

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: 2018-11-22
• Device Publish Date: 2016-04-29

Devices Manufactured by MEDTRONIC XOMED, INC.

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• 00199150023882 - N/A: 2026-02-24 PROBE 8225103 5PK PRASS SLIM PROT HANDLE
• 00763000548797 - Hydrodebrider: 2026-02-23 HYDRODEBRIDER 1914001 STD HANDPIECE ROHS
• 00763000548803 - Hydrodebrider: 2026-02-23 HANDPIECE 1921002 HYDRODEBRID FRNTL ROHS
• 20763000888910 - Merocel: 2026-02-23 PACKING 400151 100PK MICRO SPHERES 4MM
• 20763000888927 - Merocel: 2026-02-23 PACKING 400152 100PK MICRO SPHERES 5MM