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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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Embocept S DSM 50 um — 1 UDI-DI variant, MDD (Magle Chemoswed AB)

MD Atlas
Magle Chemoswed AB

Data from EUDAMED, last updated May 30, 2026

Embocept S DSM 50 um

B-07350108050012

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIb

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: Magle Chemoswed AB

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Legacy certificates

Certificate number: 144958-19-08-22
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: CE Certiso Orvos- és Kórháztechnikai Ellenőrző és Tanúsító Kft. (2409)
Validity: May 25, 2024

Identity & classification

Basic UDI-DI: B-07350108050012
Device name: Embocept S DSM 50 um
Device model: Embocept S
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Feb 27, 2024

Manufacturer & authorised representative

Manufacturer

Name: Magle Chemoswed AB
SRN: SE-MF-000003569
Country: Sweden
Email: info@maglechemoswed.com
Phone: +46 40 38 33 00

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01HQNHSPQZN7V4DWKWNB7W20N4

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

Embocept S DSM 50 um07350108050012