| Primary Device ID | 04050555000839 |
| NIH Device Record Key | 65285606-680c-4f1b-a474-acec5b418029 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MICROKERATOME Disposable Tubing |
| Version Model Number | 1 |
| Catalog Number | 5070063 |
| Company DUNS | 341325716 |
| Company Name | Technolas Perfect Vision GmbH |
| 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 | false |
| OTC Over-The-Counter | false |
| Phone | +4989940040 |
| info@technolaspv.com |
| Storage Environment Temperature | Between 5 Degrees Celsius and 35 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04050555000839 [Primary] |
| HNO | Keratome, Ac-Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-12-03 |
| Device Publish Date | 2016-09-24 |
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