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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 Ortopedia –… — 3 UDI-DI variants, MDR

MD Atlas
Surgika srl

Data from EUDAMED, last updated May 31, 2026

Pacchi procedurali per Ortopedia – Sterile procedural packs for Orthopedics

805961777PPSORTYP

3 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: 805961777PPSORTYP
Device name: —
Device model: Pacchi procedurali per Ortopedia – Sterile procedural packs for Orthopedics
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 15, 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

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRNXK69WCEFSWK49XBEJGJ6F

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

-LOWER LIMB FRACTURE SET WITH TRACTION - SET N. 2708059617773298
KNEE ARTHROSCOPY SET08059617773274
SMALL INTERVENTION SET08059617773281