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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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Conformador Perforado — 3 UDI-DI variants, MDR (AJL OPHTHALMIC, S.A)

MD Atlas
AJL OPHTHALMIC, S.A

Data from EUDAMED, last updated May 23, 2026

Conformador Perforado

84351943018SJ

3 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: AJL OPHTHALMIC, S.A

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84351943018SJ
Device name: Conformador Perforado
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: AJL OPHTHALMIC, S.A
SRN: ES-MF-000000267
Country: Spain
Email: evalarra@ajlsa.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KPX08T0YYBKRVV2VYG810HVQ

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

CF-M-AJL08435194320795
CF-L-AJL08435194320801
CF-S-AJL08435194320788