| Primary Device ID | 00721902309588 |
| NIH Device Record Key | 6f9302d1-4f69-460f-891b-2385c8366455 |
| Commercial Distribution Discontinuation | 2019-01-25 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | 5436 |
| 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 | 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 |
| Storage Environment Temperature | Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit |
| Storage Environment Temperature | Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit |
| Storage Environment Temperature | Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit |
| Storage Environment Temperature | Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00721902309588 [Primary] |
| NVZ | Pulse generator, permanent, implantable |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00721902309588]
Moist Heat or Steam Sterilization;Ethylene Oxide
[00721902309588]
Moist Heat or Steam Sterilization;Ethylene Oxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-02-18 |
| Device Publish Date | 2014-09-23 |
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| 00763000946517 - DLP® | 2024-08-12 CANNULA 70420 ART FLEX ARCH 20FR 20P 17L |