| Primary Device ID | 00810607000323 |
| NIH Device Record Key | a041cc44-e65c-40e3-a952-f457da42a1ba |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cranitomy Kit Disposable Low Speed |
| Version Model Number | 400-108 |
| Catalog Number | 400-108 |
| Company DUNS | 612611459 |
| Company Name | ACRA-CUT 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 | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| 00810607000378 | Cranitomy Kit Consisting of Qty 1 - DI810607000095 Cranial Perforator Catalog# 200-283, QTY 1 - |
| 00810607000361 | Cranitomy Kit Consisting of Qty 1 - D810607000125 Cranial Perforator Catalog# 210-221, QTY 1 - D |
| 00810607000354 | Cranitomy Kit Consisting of Qty 1 - D810607000101 Cranial Perforator Catalog# 200-331, QTY 1 - D |
| 00810607000347 | Cranitomy Kit Consisting of Qty 1 - D810607000101 Cranial Perforator Catalog# 200-331, QTY 1 - D |
| 00810607000330 | Cranitomy Kit Consisting of Qty 1 - D810607000057 Cranial Perforator Catalog# 200-253, QTY 1 - D |
| 00810607000323 | Cranitomy Kit Consisting of Qty 1 - D810607000057 Cranial Perforator Catalog# 200-253, QTY 1 - D |
| 00810607000316 | Cranitomy Kit Consisting of Qty 1 - DI810607000071 Cranial Perforator Catalog# 200-271, QTY 1 - |
| 00810607000309 | Cranitomy Kit Consisting of Qty 1 - DI 810607000019 Cranial Perforator Catalog# 200-241, QTY 1 - |