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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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430 CF M — 2 UDI-DI variants, MDR (RTS CHAPUIS)

MD Atlas
RTS CHAPUIS

Data from EUDAMED, last updated May 19, 2026

430 CF M

3770022258SERIE430PG

2 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: RTS CHAPUIS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3770022258SERIE430PG
Device name: 430 CF M
Device model: BRANCARD MONOBLOC SERIE 400
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 10, 2022

Manufacturer & authorised representative

Manufacturer

Name: RTS CHAPUIS
SRN: FR-MF-000001550
Country: France
Email: info@rtschapuis.com
Phone: + 33 04 72 48 81 82

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G2PKGRJ9AZ8MJ86VNSQ4M28Y

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

RTS CHAPUIS03770022258167
RTS CHAPUIS03770022258150