Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

ORTESI PER GINOCCHIO - GINOCCHIERE — 190 UDI-DI variants, MDR

MD Atlas
F.G.P. s.r.l.

Data from EUDAMED, last updated May 30, 2026

ORTESI PER GINOCCHIO - GINOCCHIERE

803348865Y06120902CT

190 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: F.G.P. s.r.l.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803348865Y06120902CT
Device name: ORTESI PER GINOCCHIO - GINOCCHIERE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: F.G.P. s.r.l.
SRN: IT-MF-000043862
Country: Italy
Email: jennifer.adami@fgpsrl.it
Phone: 0458600867

Variants by status

UDI-DI variants

190 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KC6864073XZYGJF9JERABM9B

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

FILAMED451V.XL08054729355882
FILAMED451V.S08054729355875
FILAMED451V.L08054729355851
FILAMED501JSV.SX.NORM.XS08033488652944
FILAMED501JIV.DX.NORM.XXL08052990112845
FILAMED501JIV.DX.NORM.M08033488652814
FILAMED501JSV.SX.NORM.L08033488652975
FILAMED501JIV.SX.NORM.M08033488652869
FILAMED501JSV.SX.NORM.XL08033488652982
FILAMED501JSV.DX.NORM.M08033488652913
FILAMED501JIV.SX.NORM.L08033488652876
FILAMED501JIV.SX.NORM.XL08033488652883
FILAMED501JIV.SX.NORM.XXL08052990112852
FILAMED501JSV.SX.NORM.M08033488652968
FILAMED501JSV.DX.NORM.XS08033488652890
FILAMED501JIV.DX.NORM.XL08033488652838
FILAMED501JIV.DX.NORM.S08033488652807
FILAMED501JSV.DX.NORM.XL08033488652937
FILAMED501JIV.DX.NORM.L08033488652821
FILAMED501JSV.DX.NORM.L08033488652920
FILAMED501JSV.SX.NORM.S08033488652951
FILAMED501JIV.SX.NORM.S08033488652852
FILAMED501JIV.DX.NORM.XS08033488652791
FILAMED501JSV.DX.NORM.S08033488652906
FILAMED501JIV.SX.NORM.XS08033488652845

1 2 3 4 5