| Primary Device ID | 00632307002212 |
| NIH Device Record Key | 167a2fdd-74a9-4166-8229-50a1dc17ce11 |
| Commercial Distribution Discontinuation | 2018-05-15 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | DMEK/DSAEK Forceps |
| Version Model Number | PD427.00 |
| Company DUNS | 622467348 |
| Company Name | PEREGRINE SURGICAL, LTD. |
| 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 | true |
| 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 |