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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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Solver — 11 UDI-DI variants, MDR (Oystershell NV)

MD Atlas
Oystershell NV

Data from EUDAMED, last updated May 23, 2026

Solver

5410765SolverRT

11 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: Oystershell NV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5410765SolverRT
Device name: Solver
Device model: X92001704
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 28, 2025

Manufacturer & authorised representative

Manufacturer

Name: Oystershell NV
SRN: BE-MF-000011797
Country: Belgium
Email: regulatory@oystershell.be
Phone: 0032.09.377.24.85

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JSXVBEFVVDR7FMQTFQ45ZP4C

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

EXCILOR EASY FR05410765005533
0701163005410765006769
0701162905410765006752
EXCILOR EASY BE NL05410765005540
0701159305410765006318
0701162805410765006745
0701152605410765005557
0701159405410765006332
0701168805410765005755
0701176105410765009784
0701176005410765009760