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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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MAGLIA MANICHE LUNGHE ANYTIME… — 2 UDI-DI variants, MDR (GOSTOLI SRL)

MD Atlas
GOSTOLI SRL

Data from EUDAMED, last updated May 30, 2026

MAGLIA MANICHE LUNGHE ANYTIME GSCLOSURE FIR CARE

805050760MLY8I94

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: GOSTOLI SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805050760MLY8I94
Device name: MAGLIA MANICHE LUNGHE ANYTIME GSCLOSURE FIR CARE
Device model: MLY8I-212359
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 3, 2026

Manufacturer & authorised representative

Manufacturer

Name: GOSTOLI SRL
SRN: IT-MF-000047997
Country: Italy
Email: marco.gostoli@gostoli.it
Phone: +39022847512

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KE22G48FSNXX9X14191CDG2Y

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

MLY8I-21235908050507601134
MLY8I-21235908050507601493