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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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TORNILLO TRANSACETABULAR DE COTILO — 6 UDI-DI variants, MDR

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

Data from EUDAMED, last updated May 23, 2026

TORNILLO TRANSACETABULAR DE COTILO

84352258IMP103000227

6 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: 84352258IMP103000227
Device name: TORNILLO TRANSACETABULAR DE COTILO
Device model: TORNILLO TRANSACETABULAR DE COTILO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jan 21, 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

6 UDI-DI variants

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Applied filters

basicUdiUlid01KFFYNGJZWN382EYQQPZ96027

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

TRANSACETABULAR CUP SCREW08435225870886
TRANSACETABULAR CUP SCREW08435225870923
TRANSACETABULAR CUP SCREW08435225870916
TRANSACETABULAR CUP SCREW08435225870909
TRANSACETABULAR CUP SCREW08435225870893
TRANSACETABULAR CUP SCREW08435225870879