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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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Bande extensible — 2 UDI-DI variants, MDR (RAFFIN MEDICAL)

MD Atlas
RAFFIN MEDICAL

Data from EUDAMED, last updated May 19, 2026

Bande extensible

3666002NSCE-BAN3-CP

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: RAFFIN MEDICAL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3666002NSCE-BAN3-CP
Device name: Bande extensible
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: RAFFIN MEDICAL
SRN: FR-MF-000004614
Country: France
Email: adv@raffin-medical.com
Phone: +33 (0)4 37 58 10 10

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J179M1ZNH5J783811B2ZDHP2

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

Bande extensible 4mx10cm03700433504379
Elastic bandage 3mx5cm03666002020827