gudid
Primary ID: D-SPECT 004
D-SPECT Refurbished (UDI D-SPECT 004)
Manufactured by SPECTRUM DYNAMICS MEDICAL, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for D-SPECT Refurbished - Primary ID D-SPECT 004
Device Regulatory Overview
The D-SPECT Refurbished (Model/Catalog Number: D-SPECT 004) is a medical device manufactured by SPECTRUM DYNAMICS MEDICAL, INC. This product is indexed under FDA Product Code / Category Classification KPS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- D-SPECT 004
- Product Code / EMDN
- KPS
- Device Name
- Single Photon Emission Computed Tomography system
- Database Sync Date
- 2026-08-09 09:18:16
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of D-SPECT Refurbished?
The registered manufacturer of record for D-SPECT Refurbished is SPECTRUM DYNAMICS MEDICAL, INC.
What is the Primary UDI-DI identifier for D-SPECT Refurbished?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-SPECT 004.
What classification code is assigned to this device?
This device is registered under product classification code KPS.
Similar Classification Devices (KPS)
Other Devices by SPECTRUM DYNAMICS MEDICAL, INC
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