gudid
Primary ID: MU-S-RP-30
DSI (UDI MU-S-RP-30)
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 MU-S-RP-30
Device Regulatory Overview
The DSI (Model/Catalog Number: MU-S-RP-30) is a medical device manufactured by D.S.I DENTAL SOLUTIONS LTD. This product is indexed under FDA Product Code / Category Classification NHA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MU-S-RP-30
- Product Code / EMDN
- NHA
- Device Name
- Premium Straight Multi-Unit Abutment 3mm
- Database Sync Date
- 2026-08-09 09:01:11
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 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 MU-S-RP-30.
What classification code is assigned to this device?
This device is registered under product classification code NHA.
Similar Classification Devices (NHA)
Other Devices by D.S.I DENTAL SOLUTIONS LTD
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