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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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Surface Coil — 30 UDI-DI variants, MDR (RAPID Biomedical GmbH)

MD Atlas
RAPID Biomedical GmbH

Data from EUDAMED, last updated May 23, 2026

Surface Coil

426048768FAMSurf_IIaKM

30 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: RAPID Biomedical GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426048768FAMSurf_IIaKM
Device name: Surface Coil
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Sep 6, 2023

Manufacturer & authorised representative

Manufacturer

Name: RAPID Biomedical GmbH
SRN: DE-MF-000008285
Country: Germany
Email: thomas.steinberger@rapidbiomed.de

Variants by status

UDI-DI variants

30 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H9N596DXZ9RENG59D6JPXKHS

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

0211304260487680713
11371305 (01882)04260487680157
45980170622104260487680546
45980170623104260487680539
45980116195204260487680010

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