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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 Cardio… — 1 UDI-DI variant, MDR (Surgika srl)

MD Atlas
Surgika srl

Data from EUDAMED, last updated May 30, 2026

Pacchi procedurali per Cardio Chirurgia – Sterile procedural packs for Cardiac Surgery

805961777PPSCARV4

1 UDI-DI variant

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: 805961777PPSCARV4
Device name: —
Device model: Pacchi procedurali per Cardio Chirurgia – Sterile procedural packs for Cardiac Surgery
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 6, 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

1 UDI-DI variant

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basicUdiUlid01KQY3ZVR0REKCAPBK5BSJQCF0

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

EMERGENCY SURGERY KIT08059617772444