Primary Device ID | 00887761996649 |
NIH Device Record Key | c2c828da-9bfd-4323-92e8-b81bf66d4e9d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Trumpf Medical |
Version Model Number | 1266933 |
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 | 00887761996649 [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 |
00887761996670 | Hospital Device |
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00887761996649 | Hospital Device |
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00887761996199 | Hospital Device |