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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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CAMILLA ELECTRICA SILVER+ — 3 UDI-DI variants, MDR (KARTSANA, S.L.)

MD Atlas
KARTSANA, S.L.

Data from EUDAMED, last updated May 23, 2026

CAMILLA ELECTRICA SILVER+

8437012914TG1200XS

3 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: KARTSANA, S.L.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8437012914TG1200XS
Device name: CAMILLA ELECTRICA SILVER+
Device model: TG-1200
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 31, 2024

Manufacturer & authorised representative

Manufacturer

Name: KARTSANA, S.L.
SRN: ES-MF-000038368
Country: Spain
Email: info@kartsana.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01HZ6HWW7AZW2GZWSS6AFD6J1V

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

TG-120008437012914117
TG-120008437012914124
TG-1200-P08437027394560