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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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BLUYAL — 4 UDI-DI variants, MDR (Fidia Farmaceutici S.p.A.)

MD Atlas
Fidia Farmaceutici S.p.A.

Data from EUDAMED, last updated May 31, 2026

BLUYAL

80336618004030100000000QE

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Fidia Farmaceutici S.p.A.

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 80336618004030100000000QE
Device name: BLUYAL
Device model: OP03-01
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Fidia Farmaceutici S.p.A.
SRN: IT-MF-000026988
Country: Italy
Email: agastaIdi@fidiapharma.it

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KSHVV0W8NA746TJGFGQH7PRP

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

1300126408055267241576
1300126308055267241651
1300126508055267241583
1300126608055267241590