INTELLIO LINK Dyonics Power II 72205189

GUDID 00885556741627

INTELLIO LINK DYONICS POWER II

Smith & Nephew, Inc.

Operating room audiovisual data/device management system application software

• Primary Device ID: 00885556741627
• NIH Device Record Key: e7bb7466-e65f-42f7-85e4-7c1ac567790a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INTELLIO LINK Dyonics Power II
• Version Model Number: 72205189
• Catalog Number: 72205189
• Company DUNS: 109903521
• Company Name: Smith & Nephew, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• 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)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556741627 [Primary]

FDA Product Code

• OUG: Medical device data system

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-03-30
• Device Publish Date: 2020-03-22

Devices Manufactured by Smith & Nephew, Inc.

• 00885556900567 - LEGION/GII: 2024-09-18 PATELLA CAPTURE ROUND/OVAL 29MM
• 00885556900574 - LEGION/GII: 2024-09-18 PATELLA CAPTURE ROUND/OVAL 32MM
• 00885556900581 - LEGION/GII: 2024-09-18 PATELLA CAPTURE ROUND/OVAL 35MM
• 00885556900598 - LEGION/GII: 2024-09-18 PATELLA CAPTURE ROUND/OVAL 38MM
• 00885556900604 - LEGION/GII: 2024-09-18 PATELLA CAPTURE ROUND/OVAL 41MM
• 00885556900611 - LEGION/GII: 2024-09-18 PATELLA CLAMP ATTACHMENT
• 00885556900628 - LEGION/GII: 2024-09-18 PATELLA SECONDARY SCREW CLAMP
• 00885556900635 - LEGION/GII: 2024-09-18 TIBIA REMOVAL TOOL