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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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SUPPORT — 8 UDI-DI variants, MDR (Tsunami Medical SRL)

MD Atlas
Tsunami Medical SRL

Data from EUDAMED, last updated May 30, 2026

SUPPORT

8055202SUPPORTSJX

8 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: Tsunami Medical SRL

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 8055202SUPPORTSJX
Device name: SUPPORT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: Tsunami Medical SRL
SRN: IT-MF-000007198
Country: Italy
Email: qara@tsunamimed.com
Phone: +39 053538397

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K6N80Y6Y6X5HBSVN2H08JZT3

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

BOK-VNT-4508055202025315
K3-72508055202009018
BOK-LT-6208055202009353
BOK-LT-TB0108055202000183
BOK-LC-6108055202009469
K3-72908055202022253
K3-72108055202009810
BOK-IDF-1008055202028149