Primary Device ID | 04059237000273 |
NIH Device Record Key | f6b9b856-da48-4cba-95d1-53b1e9a80654 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HRT3 |
Version Model Number | Rostock Cornea Module SW V1.5 |
Company DUNS | 329833875 |
Company Name | Heidelberg Engineering 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 | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |