Tumark® Professional Q for Eviva® Standard Tumark-E13-S-Q

GUDID 24250195611264

SOMATEX Medical Technologies GmbH

Imaging lesion localization marker, implantable
Primary Device ID24250195611264
NIH Device Record Keyaf269c50-e548-42a8-83ce-d9baa5181b8d
Commercial Distribution StatusIn Commercial Distribution
Brand NameTumark® Professional Q for Eviva® Standard
Version Model NumberTumark-E13-S-Q
Catalog NumberTumark-E13-S-Q
Company DUNS341679629
Company NameSOMATEX Medical Technologies GmbH
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104250195611260 [Primary]
GS114250195611267 [Package]
Contains: 04250195611260
Package: [10 Units]
In Commercial Distribution
GS124250195611264 [Package]
Contains: 14250195611267
Package: [10 Units]
In Commercial Distribution

FDA Product Code

NEUMarker, Radiographic, Implantable

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-12-27
Device Publish Date2018-11-26

On-Brand Devices [Tumark® Professional Q for Eviva® Standard]

24250195611264Tumark-E13-S-Q
14250195612080TUMARK-E13-S-Q-02

Trademark Results [Tumark]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TUMARK
TUMARK
78600901 3462258 Live/Registered
SOMATEX MEDICAL TECHNOLOGIES GMBH
2005-04-04
TUMARK
TUMARK
73670447 1476426 Dead/Cancelled
E. I. DU PONT DE NEMOURS AND COMPANY
1987-07-06

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