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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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Dispositivi monouso sterili per… — 11 UDI-DI variants, MDR

MD Atlas
MENNY MEDICAL Srl

Data from EUDAMED, last updated May 31, 2026

Dispositivi monouso sterili per infusione e accessori

805071413INFF8

11 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: MENNY MEDICAL Srl

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 805071413INFF8
Device name: Dispositivi monouso sterili per infusione e accessori
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 16, 2026

Manufacturer & authorised representative

Manufacturer

Name: MENNY MEDICAL Srl
SRN: IT-MF-000052826
Country: Italy
Email: chiara.menarini@mennymedical.it
Phone: +390535611337

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRRQ5BFY0PCJ1AF4SMB6HKZN

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

DE9090095008050714130106
DE9090091808050714130007
DE9090092008050714130045
DE9090091908050714130021
EX19311008050714130243
DE2030105908050714130144
DE9090095108050714130120
SIP101110308050714130182
DE2020102208050714130083
SIP101110208050714130069
SIP20030608050714130168