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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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DSA3500 — 2 UDI-DI variants, MDR (Dental International)

MD Atlas
Dental International

Data from EUDAMED, last updated May 30, 2026

DSA3500

87193275323DSA3500HR

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Dental International

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 87193275323DSA3500HR
Device name: DSA3500
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 8, 2022

Manufacturer & authorised representative

Manufacturer

Name: Dental International
SRN: NL-MF-000010964
Country: Netherlands
Email: info@dental.nl
Phone: +31 30 6036324

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G9YMR4NANRPRAZ38BPVD7PM0

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

DSA350008719327532294
DSA350008719327532287