| Primary Device ID | 00840113231485 |
| NIH Device Record Key | 14590b08-189f-4824-bf8d-f63276f1202a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Amnihook Amniotic Membrane Perforator |
| Version Model Number | 9601 |
| Company DUNS | 027680821 |
| Company Name | ASPEN SURGICAL PRODUCTS, 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
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| 00840113231485 - Amnihook Amniotic Membrane Perforator | 2023-03-07 Stork AmniHook, Amniotic Membrane Perforator, Yellow, Sterile, 1/pouch, 100pouches/box |
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| 00840113231546 - PlastiBell Circumcision Device | 2023-03-07 1.1 cm PlastiBell Circumcision Device |
| 00840113231560 - PlastiBell Circumcision Device | 2023-03-07 1.2 cm PlastiBell Circumcision Device |
| 00840113231577 - PlastiBell Circumcision Device | 2023-03-07 1.3 cm PlastiBell Circumcision Device |