Primary Device ID | 04056481000783 |
NIH Device Record Key | cf8ba2ea-c02a-4c15-b747-be3fcd4dc989 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Guide 4.0 Biopsy Ui |
Version Model Number | 55999-01 |
Catalog Number | 55999-01 |
Company DUNS | 314482980 |
Company Name | Brainlab AG |
Device Count | 1 |
DM Exempt | true |
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 | true |
Manufacturing Date | false |
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 |