Primary Device ID | 14250195611823 |
NIH Device Record Key | ec263f44-f8fa-4ec2-950b-e8410e27252a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tumark Conic |
Version Model Number | 351260 |
Company DUNS | 341679629 |
Company Name | SOMATEX Medical Technologies GmbH |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04250195611826 [Primary] |
GS1 | 14250195611823 [Package] Contains: 04250195611826 Package: [10 Units] In Commercial Distribution |
NEU | Marker, Radiographic, Implantable |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-10-11 |
Device Publish Date | 2021-10-01 |
14250195611830 | 351262 |
14250195611823 | 351260 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TUMARK CONIC 97001107 not registered Live/Pending |
SOMATEX MEDICAL TECHNOLOGIES GMBH 2021-08-30 |