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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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CF — 33 UDI-DI variants, MDR (VILGO)

MD Atlas
VILGO

Data from EUDAMED, last updated May 19, 2026

CF

361580CFD9

33 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: VILGO

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 361580CFD9
Device name: CF
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 1, 2026

Manufacturer & authorised representative

Manufacturer

Name: VILGO
SRN: FR-MF-000009712
Country: France
Email: vilgo@hms-vilgo.com
Phone: +33 553744550

Variants by status

UDI-DI variants

33 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KN3Z491YS3KKZAM0S3N6C83A

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

CF 0803615800001064
CF 0903615800001071
CF 1003615800001088
CF 1103615800001095
CF 1203615800001101
CF 1303615800001118
CF 1403615800001125
CF 1503615800001132
CF 1603615800001149
CF 1703615800001156
CF 1803615800045631
CF 1903615800045648
CF 2003615800045655
CF 2103615800047840
CF 2203615800047857
CF 2303615800047864
CF 2403615800047871
CF 2503615800047888
CF 2603615800047895
CF 2703615800047901
CF 2803615800047918
CF 2903615800047925
CF 3003615800052219
CF 3103615800052226
CF 3203615800052233

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