Primary Device ID | 00763000210199 |
NIH Device Record Key | 3dab35c4-8efd-493b-b679-b71261b242e0 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 3550S-01 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000210199 [Primary] |
GXR | COVER, BURR HOLE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-11-01 |
Device Publish Date | 2021-10-24 |
00763000902537 - Launcher™ | 2024-06-04 CATHETER LA83DRCD LA 8F 90CM 3DRC |
00763000902544 - Launcher™ | 2024-06-04 CATHETER LA83DRCSH LA 8F 100CM 3DRC |
00763000902551 - Launcher™ | 2024-06-04 CATHETER LA83DRCSHD LA 8F 90CM 3DRC |
00763000902568 - Launcher™ | 2024-06-04 CATHETER LA83DRIGHT LA 8F 100CM 3DRGT |
00763000902575 - Launcher™ | 2024-06-04 CATHETER LA83DRIGHTD LA 8F 90CM 3DRGT |
00763000902582 - Launcher™ | 2024-06-04 CATHETER LA8AL10 LA 8F 100CM AL10 |
00763000902599 - Launcher™ | 2024-06-04 CATHETER LA8AL10D LA 8F 90CM AL10 |
00763000902605 - Launcher™ | 2024-06-04 CATHETER LA8AL10F LA 8F 80CM AL10 |