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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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PRO METAL SW — 15 UDI-DI variants, MDR (Puma Srl)

MD Atlas
Puma Srl

Data from EUDAMED, last updated May 31, 2026

PRO METAL SW

805750785MSWZ12149002S6

15 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: Puma Srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805750785MSWZ12149002S6
Device name: PRO METAL SW
Device model: PRO METAL SW
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: Puma Srl
SRN: IT-MF-000047643
Country: Italy
Email: mauro.muselli@pumasrl.it
Phone: +39 347 3862578

Variants by status

UDI-DI variants

15 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K42P92MJ4BQ9XAME3537EJD8

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

PRO METAL SW08057507851309
PRO METAL SW08057507850593
PRO METAL SW08057507850999
PRO METAL SW08057507851323
PRO METAL SW08057507850586
PRO METAL SW08057507851293
PRO METAL SW08057507851446
PRO METAL SW08057507850982
PRO METAL SW08057507850579
PRO METAL SW08057507851248
PRO METAL SW08057507851477
PRO METAL SW08057507851286
PRO METAL SW08057507851316
PRO METAL SW08057507850562
PRO METAL SW08057507850975