Primary Device ID | 04059082010533 |
NIH Device Record Key | 0e2f325d-9811-45b4-a4d2-ae12b6bd2838 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cystoscopy obturator |
Version Model Number | 198 040 300BC |
Company DUNS | 507185952 |
Company Name | SOPRO-COMEG 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 | true |
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 | false |
OTC Over-The-Counter | false |