| Primary Device ID | 30810003222139 |
| NIH Device Record Key | 21722962-a32d-4610-bae9-9bf6f939b6b8 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | MK-600600 |
| Catalog Number | MK-600600 |
| Company DUNS | 013469890 |
| Company Name | MICROSPECIALITIES, 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx | |
| Phone | 203-874-1832 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10810003222135 [Primary] |
| GS1 | 30810003222139 [Package] Contains: 10810003222135 Package: Box [10 Units] In Commercial Distribution |
| HNO | Keratome, Ac-Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2024-02-12 |
| Device Publish Date | 2019-01-03 |
| 30810003221040 - NA | 2024-02-12 MicroKeratome Blades, Laser Calibrated HANSATOME Compatible, Plano. Have the ultimate control of corneal flap thickness while us |
| 30810003221057 - NA | 2024-02-12 MicroKeratome Blades, Laser Calibrated HANSATOME Compatible, minus 10. Have the ultimate control of corneal flap thickness while |
| 30810003221064 - NA | 2024-02-12 MicroKeratome Blades, Laser Calibrated HANSATOME Compatible, minus 20. Have the ultimate control of corneal flap thickness while |
| 30810003221071 - NA | 2024-02-12 MicroKeratome Blades, Laser Calibrated HANSATOME Compatible, minus 30. Have the ultimate control of corneal flap thickness while |
| 30810003221088 - NA | 2024-02-12 MicroKeratome Blades, Laser Calibrated HANSATOME Compatible, minus 40. Have the ultimate control of corneal flap thickness while |
| 30810003221095 - NA | 2024-02-12 MicroKeratome Blades, Laser Calibrated HANSATOME Compatible, plus 10. Have the ultimate control of corneal flap thickness while |
| 30810003221101 - NA | 2024-02-12 MicroKeratome Blades, Laser Calibrated HANSATOME Compatible, PLUS 20. Have the ultimate control of corneal flap thickness while |
| 30810003221118 - NA | 2024-02-12 MicroKeratome Blades, Laser Calibrated XP, Plano. Have the ultimate control of corneal flap thickness while using a single head |