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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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ALAMBRE DE CERCLAJE — 4 UDI-DI variants, MDR (SURGIVAL CO., S.A.U.)

MD Atlas
SURGIVAL CO., S.A.U.

Data from EUDAMED, last updated May 23, 2026

ALAMBRE DE CERCLAJE

84352258IMP30200002S

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: SURGIVAL CO., S.A.U.

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 84352258IMP30200002S
Device name: ALAMBRE DE CERCLAJE
Device model: ALAMBRE DE CERCLAJE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: SURGIVAL CO., S.A.U.
SRN: ES-MF-000028629
Country: Spain
Email: surgival@surgival.com
Phone: +34 961318050

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQVN74RMHXGTGX2NBWYX5NTG

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

CERCLAGE WIRE08435225819366
CERCLAGE WIRE08435225819373
CERCLAGE WIRE08435225819380
CERCLAGE WIRE08435225819359