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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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SpeedM® — 4 UDI-DI variants, MDR (Speed Care Mineral GmbH)

MD Atlas
Speed Care Mineral GmbH

Data from EUDAMED, last updated May 23, 2026

SpeedM®

426237786SCM001AT

4 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: Speed Care Mineral GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426237786SCM001AT
Device name: SpeedM®
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 17, 2024

Manufacturer & authorised representative

Manufacturer

Name: Speed Care Mineral GmbH
SRN: DE-MF-000020226
Country: Germany
Email: nonconformity@speedcaremineral.de
Phone: +49 395 423920

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JFAED66R4A020X0VVQVHPHJ1

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

HARTMANN TRAUMA hemostatic dressing04262377860007
NR03-XHGF-SM-0104262377860144
SpeedM®04262377860021
CG01DE04262377860045