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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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Filme Opht-R — 1 UDI-DI variant, MDD (Panin Srl)

MD Atlas
Panin Srl

Data from EUDAMED, last updated May 30, 2026

Filme Opht-R

B-08033837335047

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: Panin Srl

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: QCT-0113-19
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: ISTITUTO SUPERIORE DI SANITA' (0373)
Validity: Feb 17, 2024

Identity & classification

Basic UDI-DI: B-08033837335047
Device name: Filme Opht-R
Device model: Filme Opht-R 10 flaconi da 0.5 ml_Filme Opht-R 1 flacone 0.5 ml
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Nov 24, 2022

Manufacturer & authorised representative

Manufacturer

Name: Panin Srl
SRN: IT-MF-000020738
Country: Italy
Email: info@panin.it
Phone: +390425471323

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01GJMNR9G1467PJ409ZSE65DY8

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

Filme Opht-R08033837335047