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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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TRITON — 4 UDI-DI variants, MDR (ESTABLECIMIENTOS SUMISAN S.A.)

MD Atlas
ESTABLECIMIENTOS SUMISAN S.A.

Data from EUDAMED, last updated May 30, 2026

TRITON

8430446TRITON6B

4 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: ESTABLECIMIENTOS SUMISAN S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8430446TRITON6B
Device name: TRITON
Device model: ABS PREMIUM
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: ESTABLECIMIENTOS SUMISAN S.A.
SRN: ES-MF-000007542
Country: Spain
Email: sumisan@sumisan.com
Phone: +34 943360191

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KSMCSJPXVKEW01FQBYJ12H2V

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

ABS OP EV08430446511266
ABS ARM08430446390045
ABXL THERMO EV08430446518982
ABS PREMIUM08430446426805