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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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Hybrid Base Engaging — 2 UDI-DI variants, MDR (Elos Medtech Pinol A/S)

MD Atlas
Elos Medtech Pinol A/S

Data from EUDAMED, last updated May 23, 2026

Hybrid Base Engaging

5712821007001VC

2 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: Elos Medtech Pinol A/S

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 5712821007001VC
Device name: Hybrid Base Engaging
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Elos Medtech Pinol A/S
SRN: DK-MF-000001915
Country: Denmark
Email: lise.terkelsen@elosmedtech.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KR0THQD0PYRMM8M9BYWBR5Z8

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

Elos Accurate® Hybrid Base™ Engaging05712821000309
Elos Accurate® Hybrid Base™ Engaging05712821000316