| Primary Device ID | 00810607000125 |
| NIH Device Record Key | 2b64c87c-8247-4bbe-b9e8-784712fcbfd8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Disposable Cranial Perforator |
| Version Model Number | 210-221 14/11 mm |
| Catalog Number | 210-221 CDM |
| Company DUNS | 612611459 |
| Company Name | ACRA-CUT 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | 9782632210 |
| info@acracut.com | |
| Phone | 9782632210 |
| info@acracut.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810607000125 [Primary] |
| HBF | Drills, Burrs, Trephines & Accessories (Compound, Powered) |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[00810607000125]
Radiation Sterilization
[00810607000125]
Radiation Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-05-01 |
| 00810607000125 | Cranial Perforator |
| 00810607000118 | Cranial Perforator |
| 00810607000101 | Cranial Perforator |
| 00810607000095 | Cranial Perforator |
| 00810607000088 | Cranial Perforator |
| 00810607000071 | Cranial Perforator |
| 00810607000064 | Cranial Perforator |
| 00810607000057 | Cranial Perforator |
| 00810607000040 | Cranial Perforator |
| 00810607000033 | Cranial Perforator |
| 00810607000026 | Cranial Perforator |
| 00810607000019 | Cranial Perforator |