Primary Device ID | 00721902620898 |
NIH Device Record Key | cc5ee941-438d-4d95-9bbf-a285c61fea1c |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 8586 |
Company DUNS | 796986144 |
Company Name | MEDTRONIC, 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 | 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 | true |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Length | 38 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00721902620898 [Primary] |
LKK | PUMP, INFUSION, IMPLANTED, PROGRAMMABLE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2014-09-23 |
00199150000012 - NA | 2025-03-07 CUSTOM PACK BB10J80R7 1/4CNTRI |
00763000997984 - NA | 2025-03-07 CUSTOM PACK BB11F56R9 PEDS V |
00763000999346 - NA | 2025-03-07 CUSTOM PACK BB3R67R6 SU AVLOOP |
20763000999364 - NA | 2025-03-07 CUSTOM PACK BB8A42R1 2PK TAVR PACK |
20763000999388 - NA | 2025-03-07 CUSTOM PACK BB3J83R2 5PK 38X332X16 |
20763000999401 - NA | 2025-03-07 CUSTOM PACK BB11J01R1 5PK BRIDGE SUP |
00763000999513 - NA | 2025-03-07 CUSTOM PACK BB11F41R3 ADLT SUPP PAC |
20763000999777 - NA | 2025-03-07 CUSTOM PACK BB12M84R1 10PK 3/8 SUPP LINE |