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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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Silcap Shampoo I — 3 UDI-DI variants, MDR (Oystershell NV)

MD Atlas
Oystershell NV

Data from EUDAMED, last updated May 23, 2026

Silcap Shampoo I

5410765SilcapShampooG5

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Oystershell NV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5410765SilcapShampooG5
Device name: Silcap Shampoo I
Device model: X92001086
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 8, 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

3 UDI-DI variants

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Applied filters

basicUdiUlid01JTQKV0C2MKWVV34S7KZPG92P

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

0701078205410765003454
0701078105410765003447
0703089705410765007285