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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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TRIPOD — 7 UDI-DI variants, MDR (FDI FRANCE)

MD Atlas
FDI FRANCE

Data from EUDAMED, last updated May 19, 2026

TRIPOD

3665155AccCan8T

7 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: FDI FRANCE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3665155AccCan8T
Device name: TRIPOD
Device model: TRIPOD
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 11, 2023

Manufacturer & authorised representative

Manufacturer

Name: FDI FRANCE
SRN: FR-MF-000023166
Country: France
Email: contact@fdifrance.com
Phone: +33 4 76 32 27 33

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01H05GV3H1KSWXXKQ3DA685ZDM

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

TR/05/0703665155001080
WS/06/0203665155001288
WS/02/0203665155001264
WS/07/0203665155001271
WS/02/0503665155001325
WS/02/0503665155001301
WS/07/0503665155001318