Primary Device ID | 00643169312081 |
NIH Device Record Key | 08e89014-a657-4735-9abc-11a96278a8da |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MEDTRONIC CARELINK EXPRESS™ |
Version Model Number | 2020C2 |
Company DUNS | 006261481 |
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 | 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 |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Storage Environment Temperature | Between -40 Degrees Fahrenheit and 150 Degrees Fahrenheit |
Storage Environment Temperature | Between -40 Degrees Fahrenheit and 150 Degrees Fahrenheit |
Storage Environment Temperature | Between -40 Degrees Fahrenheit and 150 Degrees Fahrenheit |
Storage Environment Temperature | Between -40 Degrees Fahrenheit and 150 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169312081 [Primary] |
NVZ | Pulse generator, permanent, implantable |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-12-23 |
00613994952431 | MON 2020C1 CARELINK USA EXPRESS MONITOR |
00613994952400 | MON 2020B1 CARELINK USA EXPRESS MONITOR |
00643169107052 | MON 2020B2 CARELINK USA MR4 MONITOR |
00643169312081 | MON 2020C2 CARELINK 60601 3ED USA |
00643169192058 | MON 2020B3 CARELINK USA BW 60601 |