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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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Pacchi procedurali per Urologia –… — 5 UDI-DI variants, MDR

MD Atlas
Surgika srl

Data from EUDAMED, last updated May 31, 2026

Pacchi procedurali per Urologia – Sterile procedural packs for Urology

805961777PPSUROZB

5 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Surgika srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805961777PPSUROZB
Device name: —
Device model: Pacchi procedurali per Urologia – Sterile procedural packs for Urology
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Surgika srl
SRN: IT-MF-000024206
Country: Italy
Email: info@surgika.it
Phone: +39 055 9180204

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KRWZEVGR6NVS8Q75VE2DYY5C

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

SET FOR TURV - TURP - SET N° 2808059617773359
TURP UROLOGY KIT 108053178797137
TURP UROLOGY KIT 208053178796765
UROLOGICAL SURGERY KIT08059617773366
UROLOGY KIT08059617773397