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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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ORTESI CERVICALI (COLLARI) - RACHIDE… — 34 UDI-DI variants, MDR

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

Data from EUDAMED, last updated May 31, 2026

ORTESI CERVICALI (COLLARI) - RACHIDE CERVICALE

803348865Y06031201BT

34 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.

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UDI-DI variants

34 UDI-DI variants

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Applied filters

basicUdiUlid01JV9BPGG7JQ8P093SHH2K7VWT

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

CLC-100/10V.S08033488650315
CLC-100/6V.M08033488650384
CLC-100/6V.L08033488650391
CLC-100/8V.L08033488650421
CLC-100/6V.XL08052990119646
CLC-100/10V.M08033488650322
CLC-100/8V.S08033488650407
CLC-100/6V.S08033488650377
CLC-100/8V.XL08052990119653
CLC-100/10V.XL08052990119639
CLC-100/8V.M08033488650414
CLC-100/10V.L08033488650339
CLL-300V.3°08033488650469
CLL-300V.0°08033488650438
CLL-300V.1°08033488650445
CLL-300V.4°08033488650476
CLL-300V.2°08033488650452
CLL-901/3V.L08033488650698
CLL-901/3V.M08033488650681
CLL-901/5V.L08033488650759
CLL-901/4V.L08033488650728
CLL-901/2V.M08033488650650
CLL-901/4V.S08033488650704
CLL-901/2V.L08033488650667
CLL-901/4V.M08033488650711

1 2

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803348865Y06031201BT
Device name: ORTESI CERVICALI (COLLARI) - RACHIDE CERVICALE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 27, 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