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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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Avvero Lenti — 4 UDI-DI variants, MDR (AVVERO LENTI SRL)

MD Atlas
AVVERO LENTI SRL

Data from EUDAMED, last updated May 30, 2026

Avvero Lenti

59447571LENTILEOCHELARI9X

4 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: AVVERO LENTI SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 59447571LENTILEOCHELARI9X
Device name: Avvero Lenti
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 4, 2022

Manufacturer & authorised representative

Manufacturer

Name: AVVERO LENTI SRL
SRN: RO-MF-000021241
Country: Romania
Email: contact@avvero.ro
Phone: 0040743221122

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01FZSH8TBN44KZSPEZQKWG7JX2

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

AVVEROBIFO05944757100031
AVVERODEGR05944757100000
AVVEROPROG05944757100024
AVVEROMONO05944757100017