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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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INSCREW — 11 UDI-DI variants, MDR (Tsunami Medical SRL)

MD Atlas
Tsunami Medical SRL

Data from EUDAMED, last updated May 31, 2026

INSCREW

8055202INSCREWWL

11 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: 8055202INSCREWWL
Device name: INSCREW
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 10, 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

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K76G1NXJR0XFWPY3GS5SQK8Q

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-2008055202025070
BOK-VNT-0908055202025018
BOK-VNT-0808055202025001
BOK-VNT-0708055202024998
BOK-VNT-1908055202025063
BOK-VNT-2508055202025124
BOK-VNT-3408055202025216
BOK-VNT-2808055202025155
BOK-VNT-2208055202025094
BOK-VNT-2908055202025162
BOK-VNT-0508055202024974