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

GUDID 24250195611264

SOMATEX Medical Technologies GmbH

Imaging lesion localization marker, implantable

• Primary Device ID: 24250195611264
• NIH Device Record Key: af269c50-e548-42a8-83ce-d9baa5181b8d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tumark® Professional Q for Eviva® Standard
• Version Model Number: Tumark-E13-S-Q
• Catalog Number: Tumark-E13-S-Q
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	04250195611260 [Primary]
GS1	14250195611267 [Package]; Contains: 04250195611260; Package: [10 Units]; In Commercial Distribution
GS1	24250195611264 [Package]; Contains: 14250195611267; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• NEU: Marker, Radiographic, Implantable

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-12-27
• Device Publish Date: 2018-11-26

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

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