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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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Fibrafill® CUBE — 2 UDI-DI variants, MDR (ADM, a.s.)

MD Atlas
ADM, a.s.

Data from EUDAMED, last updated May 23, 2026

Fibrafill® CUBE

85956527CUBE25

2 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: ADM, a.s.

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 85956527CUBE25
Device name: Fibrafill® CUBE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: ADM, a.s.
SRN: CZ-MF-000032589
Country: Czechia
Email: bystricky@dentapreg.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K3TEKS1JNE7A8YRCYSDXG4C6

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

F-00108595652700641
F-10108595652700696