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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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HOLDER — 67 UDI-DI variants, MDR (Tsunami Medical SRL)

MD Atlas
Tsunami Medical SRL

Data from EUDAMED, last updated May 31, 2026

HOLDER

8055202HOLDERRP

67 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: 8055202HOLDERRP
Device name: HOLDER
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 30, 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

67 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K6DA709Y3HT81X5B6AKGBZ2C

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

ZURI100208055202036472
BOK-LDH-0208055202027258
BOK-VNT-0108055202024936
BOK-GL-01-0108055202036151
BOK-VNT-3008055202025179
BOK-CSZ-0308055202026886
BOK-CS-0108055202022109
BOK-LCH-0208055202026978
BOK-VNT-2108055202025087
BOK-ACA-0208055202008981
BOK-LD-02S08055202035741
BOK-CSZ-0508055202036250
BOK-LD-01TB08055202029405
BOK-LD-02B08055202019031
BOK-LTH-0208055202022048
BOK-IDF-0108055202036175
BOK-LD-02TB08055202028538

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