| Primary Device ID | 07290112447371 |
| NIH Device Record Key | e1125253-ce8c-4e48-83dc-1dab95d73733 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Guide Pin |
| Version Model Number | ET-0102 |
| Company DUNS | 514570324 |
| Company Name | ETGAR - MEDICAL INSTRUMENTS LTD |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |