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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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MicroREC 3D — 8 UDI-DI variants, MDR (Custom Surgical GmbH)

MD Atlas
Custom Surgical GmbH

Data from EUDAMED, last updated May 23, 2026

MicroREC 3D

426073827MRC3D9T

8 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: Custom Surgical GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426073827MRC3D9T
Device name: MicroREC 3D
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: Custom Surgical GmbH
SRN: DE-MF-000034959
Country: Germany
Email: regulatory@customsurgical.co

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMD3KRZCP6SYX71GS36HV4TP

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

MicroREC 3D04260738270434
MicroREC 3D04260738270472
MicroREC 3D04260738270496
MicroREC 3D04260738270458
MicroREC 3D04260738270427
MicroREC 3D04260738270465
MicroREC 3D04260738270441
MicroREC 3D04260738270489