Sil-serter™

GUDID 00763000381080

LANCET MMT-385 SILSERTER MDR

MEDTRONIC MINIMED, INC.

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• Primary Device ID: 00763000381080
• NIH Device Record Key: 67754fc5-877b-483b-947f-3a3d61a42cc8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sil-serter™
• Version Model Number: MMT-385
• Company DUNS: 849626338
• Company Name: MEDTRONIC MINIMED, 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
• 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	00763000381080 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K010377

FDA Product Code

• KZH: INTRODUCER, SYRINGE NEEDLE

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: 2021-04-30
• Device Publish Date: 2021-04-22

Devices Manufactured by MEDTRONIC MINIMED, INC.

• 00763000924089 - MiniMed™ 780G: 2024-06-17 PUMP MMT-1884 780G US MG A2.01 6.21U
• 00763000924096 - MiniMed™ 780G: 2024-06-17 PUMP MMT-1884 780G US A2.01 6.21U PRB
• 00763000924102 - MiniMed™ 780G: 2024-06-17 KIT MMT-1894 780G US MG A2.01 6.21U
• 00763000924119 - MiniMed™ 780G: 2024-06-17 KIT MMT-1894MD 780G US A2.01 6.21U
• 00763000827182 - inpen™: 2024-06-11 KIT MMT-105NNBLNA INPEN NOVONORDISK BLUE
• 00763000827199 - inpen™: 2024-06-11 KIT MMT-105NNGYNA INPEN NOVONORDISK GREY
• 00763000827205 - inpen™: 2024-06-11 KIT MMT-105NNPKNA INPEN NOVONORDISK PINK
• 00763000827151 - inpen™: 2024-06-10 KIT MMT-105ELBLNA INPEN ELI LILLY BLUE