gudid Primary ID: AL203-PP

DSI Adastra Paste (UDI AL203-PP)

Manufactured by D.S.I DENTAL SOLUTIONS LTD

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The DSI Adastra Paste (Model/Catalog Number: AL203-PP) is a medical device manufactured by D.S.I DENTAL SOLUTIONS LTD. This product is indexed under FDA Product Code / Category Classification EJR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: AL203-PP
Product Code / EMDN: EJR
Device Name
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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Frequently Asked Questions

Who is the primary manufacturer of DSI Adastra Paste?

The registered manufacturer of record for DSI Adastra Paste is D.S.I DENTAL SOLUTIONS LTD.

What is the Primary UDI-DI identifier for DSI Adastra Paste?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AL203-PP.

What classification code is assigned to this device?

This device is registered under product classification code EJR.

Similar Classification Devices (EJR)

Other Devices by D.S.I DENTAL SOLUTIONS LTD

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