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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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MAGIC Microcatheter — 9 UDI-DI variants, MDR (Balt extrusion SAS)

MD Atlas
Balt extrusion SAS

Data from EUDAMED, last updated May 19, 2026

MAGIC Microcatheter

03700481300122

9 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class III

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Manufacturer: Balt extrusion SAS

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 170779129
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: DQS Medizinprodukte GmbH (0297)
Validity: Sep 2, 2022 → Sep 1, 2027

Identity & classification

Basic UDI-DI: 03700481300122
Device name: MAGIC Microcatheter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: May 2, 2023

Manufacturer & authorised representative

Manufacturer

Name: Balt extrusion SAS
SRN: FR-MF-000007563
Country: France
Email: PRRC@baltgroup.com
Phone: +33 (0)1 39 89 46 41

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01GWRSG6DR4GMWJ2J3RBW07D0J

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

MAGIC1.2FM18003700481338308
MAGICSTD03700481338391
MA1.2FOLIVE03700481338292
MAGIC1,2F03700481345382
MAGIC1.5F03700481338339
MAGIC1.2FM03700481338315
MA1.5FOLIVEMP03700481338322
MA1.5FMP03700481338384
MAGICMP03700481338377