gudid
Primary ID: SPI1038
DSI (UDI SPI1038)
Manufactured by D.S.I DENTAL SOLUTIONS LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DSI - Primary ID SPI1038
Device Regulatory Overview
The DSI (Model/Catalog Number: SPI1038) is a medical device manufactured by D.S.I DENTAL SOLUTIONS LTD. This product is indexed under FDA Product Code / Category Classification DZE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SPI1038
- Product Code / EMDN
- DZE
- Device Name
- Premium Spiral Implant 3.75 x 10 mm
- Database Sync Date
- 2026-08-09 09:01:11
Full Regulatory Attributes
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{
"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 DSI?
The registered manufacturer of record for DSI is D.S.I DENTAL SOLUTIONS LTD.
What is the Primary UDI-DI identifier for DSI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SPI1038.
What classification code is assigned to this device?
This device is registered under product classification code DZE.
Similar Classification Devices (DZE)
Other Devices by D.S.I DENTAL SOLUTIONS LTD
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