D-SPECT Refurbished 8010517-01

GUDID 07290108670523

Single Photon Emission Computed Tomography system

SPECTRUM DYNAMICS MEDICAL, INC

SPECT system, annular detector array

• Primary Device ID: 07290108670523
• NIH Device Record Key: 60c09bb9-5a1e-44db-b58c-055707887122
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: D-SPECT Refurbished
• Version Model Number: D-SPECT 002
• Catalog Number: 8010517-01
• Company DUNS: 078864620
• Company Name: SPECTRUM DYNAMICS MEDICAL, INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290108670523 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K161740

FDA Product Code

• KPS: System, Tomography, Computed, Emission

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-02-17
• Device Publish Date: 2026-02-09

On-Brand Devices [D-SPECT Refurbished]

• 00729018670158: Single Photon Emission Computed Tomography system
• 07290108670158: Single Photon Emission Computed Tomography system
• 07290108670097: The D-SPECT® system is a single photon emission computing tomography system (SPECT) intended fo
• 07290108670523: Single Photon Emission Computed Tomography system