OCTOPUS®

GUDID 00643169668911

STABILIZER TS2000 OCTOPUS EVOLUTION 16L

MEDTRONIC, INC.

Patient positioning vacuum pad

• Primary Device ID: 00643169668911
• NIH Device Record Key: 03b612c8-7f4a-4f22-8525-5f8ac1934ad4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OCTOPUS®
• Version Model Number: TS2000
• Company DUNS: 006261481
• Company Name: MEDTRONIC, INC.
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169668911 [Primary]

FDA Product Code

• MWS: stabilizer,heart

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-07-08

On-Brand Devices [OCTOPUS®]

• 00643169668973: TISSUE STABILIZER TS102 NON-STERNOTOMY
• 00643169668966: TISSUE STABILIZER TS102 NON-STERNOTOMY
• 00643169668959: STABILIZER TSMICS1 OCTOPUS NUVO 26L
• 00643169668942: STABILIZER TSMICS1 OCTOPUS NUVO 26L
• 00643169668928: TISSUE STABILIZER 29403 OCTOPUS 4.3 16L
• 00643169668911: STABILIZER TS2000 OCTOPUS EVOLUTION 16L
• 00643169668904: STABILIZER TS2500 OCTO EVOLUTION AS 26L
• 00885074099835: TISSUE STABILIZER 29400 OCTOPUS 4 16L
• 00763000543693: STABILIZER TSMICS1 OCTOPUS NUVO 26L
• 00763000543679: STABILIZER 29400 OCTOPUS 4 16L