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

FILAMED701 WRAP ARV.XS08052990112708
FILAMED701 WRAP ARV.XL08052990112692
FILAMED701 WRAP ARV.C/MIS08052990112654
FILAMED701 WRAP ARV.L08052990112661
FILAMED701 WRAP ARV.M08052990112678
FILAMED701 WRAP ARV.XXL08052990112715
FILAMED851V.NORM.M08033488653286
FILAMED851V.NORM.XL08033488653309
FILAMED851V.NORM.S08033488653279
FILAMED851V.NORM.L08033488653293
0803348865326208033488653262
FILAMED801V.NORM.XS08033488653217
FILAMED801V.NORM.L08033488653248
FILAMED801V.NORM.S08033488653224
FILAMED801V.NORM.XL08033488653255
FILAMED801V.NORM.M08033488653231
0805472935660508054729356605
0805472935659908054729356599
FFK-400V.XS08054729356629
0805472935661208054729356612
FFK-400V.XXL08054729356636
0805472935658208054729356582
KIDZ-TEKV.M08052990114450
KIDZ-TEKV.L08052990114443
KIDZ-TEKV.S08052990114467

2 3 4 5 6