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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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HAMMER — 4 UDI-DI variants, MDR (Tsunami Medical SRL)

MD Atlas
Tsunami Medical SRL

Data from EUDAMED, last updated May 31, 2026

HAMMER

8055202HAMMERSPU

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: Tsunami Medical SRL

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 8055202HAMMERSPU
Device name: HAMMER
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

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K6MJ79XXDR7KC0VVGN7KE1TP

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-LD-0308055202009735
TH00208055202009780
BOK-LT-8008055202009476
BOK-LC-5908055202009322