Sentimag SMB03

GUDID 15060391210312

Sentimag Gen 3 Base Unit

ENDOMAGNETICS LTD

Magnetic metal detector

• Primary Device ID: 15060391210312
• NIH Device Record Key: 225de6d6-30a6-4bc7-8d60-1d1cc0f3dfad
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sentimag
• Version Model Number: Gen 3
• Catalog Number: SMB03
• Company DUNS: 846963171
• Company Name: ENDOMAGNETICS LTD
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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	15060391210312 [Primary]

FDA Product Code

• NEU: Marker, Radiographic, Implantable

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-03-22
• Device Publish Date: 2024-02-09

On-Brand Devices [Sentimag]

• 15060391210350: Thin Probe for Sentimag Gen 3
• 15060391210312: Sentimag Gen 3 Base Unit
• 15060391210343: Probe checker for Sentimag Gen 3 Probe
• 15060391210336: Footswitch for Sentimag Gen 3
• 15060391210329: Standard Probe for Sentimag Gen 3