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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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SYMMED SMART HANDPIECE RES — 2 UDI-DI variants, MDR (Termosalud, S.L.)

MD Atlas
Termosalud, S.L.

Data from EUDAMED, last updated May 23, 2026

SYMMED SMART HANDPIECE RES

843660129SSHPRES2R

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Termosalud, S.L.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 843660129SSHPRES2R
Device name: SYMMED SMART HANDPIECE RES
Device model: SYMMED SMART HANDPIECE RES
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Feb 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: Termosalud, S.L.
SRN: ES-MF-000019177
Country: Spain
Email: regulatory@termosalud.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KGM59D8Z2MEK96ZP0ZBP6GGZ

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

A487AE08436601290434
A487N08436601290250