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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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MANIGLIONE/CORRIMANO — 5 UDI-DI variants, MDR (PONTE GIULIO S.P.A.)

MD Atlas
PONTE GIULIO S.P.A.

Data from EUDAMED, last updated Jun 2, 2026

MANIGLIONE/CORRIMANO

80218800000000009UF

5 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: PONTE GIULIO S.P.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 80218800000000009UF
Device name: MANIGLIONE/CORRIMANO
Device model: MANIGLIONE/CORRIMANO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 1, 2026

Manufacturer & authorised representative

Manufacturer

Name: PONTE GIULIO S.P.A.
SRN: IT-MF-000010424
Country: Italy
Email: info@pontegiulio.it
Phone: 0763 316044

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KT13CV04TDX6RJ8MKVK4KCZN

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

G01JBS17W108023616007821
G40JAS18W108023616143307
G01JBS18W108023616007838
G01JAS18W108023616005599
G01JAS17W108023616005582