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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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Non sterile hard contact lenses — 1 UDI-DI variant, MDD

MD Atlas
UCO - Lavec BV

Data from EUDAMED, last updated May 31, 2026

Non sterile hard contact lenses

B-872086507HARDHKGV

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: UCO - Lavec BV

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Legacy certificates

Certificate number: BE19/819943762
Type: refdata.legacy.mdd-certificate-type.v
Notified body: SGS Belgium NV (1639)
Validity: May 24, 2024

Identity & classification

Basic UDI-DI: B-872086507HARDHKGV
Device name: Non sterile hard contact lenses
Device model: Non sterile hard contact lenses
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Nov 25, 2025

Manufacturer & authorised representative

Manufacturer

Name: UCO - Lavec BV
SRN: NL-MF-000011698
Country: Netherlands
Email: info@ucocontactlenzen.nl
Phone: +31227601837

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KAX1MSJ5GY7665XREE6E1RBH

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

Non-sterile hard contact lensesD-872086507HARDHKGV