Primary Device ID | 00887761996069 |
NIH Device Record Key | cb38c0a2-2a4c-40f1-ad12-18f577e82119 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TruSystem |
Version Model Number | 1854085 |
Company DUNS | 330961223 |
Company Name | TRUMPF Medizin Systeme GmbH + Co. KG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 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 |
Phone | +49367158641911 |
service.wwo@trumpfmedical.com | |
Phone | +49367158641911 |
service.wwo@trumpfmedical.com | |
Phone | +49367158641911 |
service.wwo@trumpfmedical.com | |
Phone | +49367158641911 |
service.wwo@trumpfmedical.com | |
Phone | +49367158641911 |
service.wwo@trumpfmedical.com | |
Phone | +49367158641911 |
service.wwo@trumpfmedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887761996069 [Primary] |
KXJ | Table, radiologic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-17 |
00887761996229 | Hospital Device |
00887761996069 | Hospital Device |
00887761996052 | Hospital Device |
00887761996045 | Hospital Device |
00887761996038 | Hospital Device |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TRUSYSTEM 76688060 4028979 Live/Registered |
TRUMPF GMBH + CO. KG 2008-03-26 |