Primary Device ID | 04250435501344 |
NIH Device Record Key | bc7261f7-a651-44c6-bf47-81285edca2f7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DORO LUCENT® Headplate |
Version Model Number | 3010-00 |
Catalog Number | 3010-00 |
Company DUNS | 313517922 |
Company Name | pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04250435501344 [Primary] |
HBL | Holder, Head, Neurosurgical (Skull Clamp) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-12-27 |
Device Publish Date | 2018-11-26 |
04250435532140 | DORO LUCENT® Headplate |
04250435501344 | DORO® Table Adapter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DORO LUCENT 79151055 4929537 Live/Registered |
pro med instruments GmbH Herstellung un 2014-06-27 |