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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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Ophthalmic syringes — 2 UDI-DI variants, MDR (FIMCO)

MD Atlas
FIMCO

Data from EUDAMED, last updated May 19, 2026

Ophthalmic syringes

3665857FAM0303P4

2 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: FIMCO

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 3665857FAM0303P4
Device name: Ophthalmic syringes
Device model: Manual syringes with Luer connection intended for aspiration and injection of fluids in ophthalmic procedures, various volumes
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: FIMCO
SRN: FR-MF-000000175
Country: France
Email: contact.website@fimco-france.com
Phone: +33 4 68 83 32 35

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KR19CX9VF9C276907AD3VDDF

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

Luer syringe, 3 cc03665857005676
Luer syringe, 5 cc03665857005683