MiniMed® 670G

GUDID 00643169939202

PUMP MMT-1780K 670G V3.18 BK SF MG

MEDTRONIC MINIMED, INC.

Ambulatory insulin infusion pump, electronic

• Primary Device ID: 00643169939202
• NIH Device Record Key: bc2fc8f7-2512-461e-8db5-0864665c6de6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MiniMed® 670G
• Version Model Number: MMT-1780K
• Company DUNS: 849626338
• Company Name: MEDTRONIC MINIMED, INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• 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)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

Operating and Storage Conditions

• Storage Environment Humidity: Between 5 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 5 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 5 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 5 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
• Storage Environment Temperature: Between -20 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Humidity: Between 5 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
• Storage Environment Temperature: Between -20 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Humidity: Between 5 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169939202 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P160017

FDA Product Code

• OZP: Artificial pancreas device system, single hormonal control

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-09-12
• Device Publish Date: 2017-03-30

On-Brand Devices [MiniMed® 670G]

• 00643169946057: KIT MMT-1760KPK 670G V3.18 EN MG
• 00643169946040: KIT MMT-1760K 670G REV V3.18 EN MG
• 00643169939219: PUMP MMT-1780KPK 670G V3.18 EN MG
• 00643169939202: PUMP MMT-1780K 670G V3.18 BK SF MG
• 00763000179649: KIT MMT-1760KP 670G 3ML V4.10 EN PW
• 00763000173043: PUMP MMT-1780KP 670G V4.10 SF MG PW
• 00763000166526: PUMP MMT-1780KL 670G V4.10 BK SF MG
• 00763000157050: KIT MMT-1760KPK 670G V4.10 EN MG
• 00763000075460: PUMP MMT-1780KP 670G V3.18 BK SF MG
• 00763000075453: KIT MMT-1760KP 670G 3ML V3.18 BK EN
• 00763000072537: PUMP MMT-1780KL 670G V3.18 BK SF MG
• 00763000256838: PUMP MMT-1780KP 670G V4.11 JBL MG PW
• 00763000256821: PUMP MMT-1780KL 670G V4.11 JBL MG
• 00763000278427: KIT MMT-1760KM 670G V4.11 MG NR
• 00763000293888: PUMP MMT-1780KR 670G V4.10 MG RECERT
• 00763000293871: KIT MMT-1760KR 670G V4.10 MG
• 00763000283520: PUMP MMT-1780KPK 670G V4.11 MG
• 00763000283513: PUMP MMT-1780KL 670G V4.11 JBL MG
• 00763000283506: PUMP MMT-1780KL 670G V4.10 BM MG
• 00763000283445: KIT MMT-1760KPK 670G V4.11 MG
• 00763000190460: PUMP MMT-1780KPK 670G V4.11 EN MG
• 00763000190453: KIT MMT-1760KPK 670G V4.11 EN MG
• 00763000367084: KIT MMT-1760KR 670G V4.11 JBL MG
• 00763000365929: PUMP MMT-1780KM 670G V4.11 JBL MG
• 00763000365912: PUMP MMT-1780KR 670G V4.11 MG JBL RECERT
• 00763000365882: PUMP MMT-1780KL 670G V4.11 JBL MG
• 00763000367077: KIT MMT-1760KM 670G V4.11 MG
• 00763000395858: KIT MMT-1760KPK 670G V4.11 PRB MG
• 00763000393786: PUMP MMT-1780KPK 670G V4.11 PRB MG