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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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MONOGIN SOLUZIONE — 10 UDI-DI variants, MDR (LO.LI. PHARMA S.r.l.)

MD Atlas
LO.LI. PHARMA S.r.l.

Data from EUDAMED, last updated May 30, 2026

MONOGIN SOLUZIONE

805848125MONOGINsoluzNX

10 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: LO.LI. PHARMA S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805848125MONOGINsoluzNX
Device name: MONOGIN SOLUZIONE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: LO.LI. PHARMA S.r.l.
SRN: IT-MF-000023734
Country: Italy
Email: info@lolipharma.it
Phone: +39 06 22442074

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01JPHPEWBDMBP8F6S82DCKCDVG

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

BIGUANELLE08058481250157
BIGUANELLE08058481251291
BIGUANELLE08058481250867
BIGUANELLE08058481251222
BIGUANELLE08058481250171
CLOTIDAL TOTAL08058481251307
CLOTIDAL TOTAL08058481251161
EVAGYNAL08058481250225
MELAGYN08058481250232
MONOGIN SOLUZIONE08058481250126