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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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RYM NASAL GEL — 1 UDI-DI variant, MDR (Fidia Farmaceutici S.p.A.)

MD Atlas
Fidia Farmaceutici S.p.A.

Data from EUDAMED, last updated May 30, 2026

RYM NASAL GEL

80336618006060100000000VV

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
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: 80336618006060100000000VV
Device name: RYM NASAL GEL
Device model: MC06-01
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 30, 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

1 UDI-DI variant

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Applied filters

basicUdiUlid01KQF9J123CQCYAWM9NQCMFDF6

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

1300120908055267242924