| Primary Device ID | 00763000140045 |
| NIH Device Record Key | 27d15d92-15d0-4b9d-8f81-bde3f76181f1 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 9564035 |
| Company DUNS | 830350380 |
| Company Name | MEDTRONIC SOFAMOR DANEK, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | true |
| 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 |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000140045 [Primary] |
| GAD | RETRACTOR |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00763000140045]
Moist Heat or Steam Sterilization
[00763000140045]
Moist Heat or Steam Sterilization
[00763000140045]
Moist Heat or Steam Sterilization
[00763000140045]
Moist Heat or Steam Sterilization
[00763000140045]
Moist Heat or Steam Sterilization
[00763000140045]
Moist Heat or Steam Sterilization
[00763000140045]
Moist Heat or Steam Sterilization
[00763000140045]
Moist Heat or Steam Sterilization
[00763000140045]
Moist Heat or Steam Sterilization
[00763000140045]
Moist Heat or Steam Sterilization
[00763000140045]
Moist Heat or Steam Sterilization
[00763000140045]
Moist Heat or Steam Sterilization
[00763000140045]
Moist Heat or Steam Sterilization
[00763000140045]
Moist Heat or Steam Sterilization
[00763000140045]
Moist Heat or Steam Sterilization
[00763000140045]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-10-04 |
| Device Publish Date | 2021-09-24 |
| 00763000764050 - OsteoCool™ 2.0 RF Ablation System | 2024-11-19 CART OCA01-100 OC 2.0 100W STAND |
| 00763000670542 - n/a | 2024-11-18 TEMPLATE 3005975 ZEVO 75MM 5 LVL |
| 00763000670559 - n/a | 2024-11-18 TEMPLATE 3005977 ZEVO 77MM 5 LVL |
| 00763000670566 - n/a | 2024-11-18 TEMPLATE 3005979 ZEVO 79MM 5 LVL |
| 00763000670573 - n/a | 2024-11-18 TEMPLATE 3005981 ZEVO 81MM 5 LVL |
| 00763000670580 - n/a | 2024-11-18 TEMPLATE 3005985 ZEVO 85MM 5 LVL |
| 00763000670597 - n/a | 2024-11-18 TEMPLATE 3005990 ZEVO 90MM 5 LVL |
| 00763000670603 - n/a | 2024-11-18 TEMPLATE 3005995 ZEVO 95MM 5 LVL |