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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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Dentapreg® PFU — 8 UDI-DI variants, MDR (ADM, a.s.)

MD Atlas
ADM, a.s.

Data from EUDAMED, last updated May 23, 2026

Dentapreg® PFU

85956527PFU9J

8 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: 85956527PFU9J
Device name: Dentapreg® PFU
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 28, 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

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K3R5651VM535TFTZCGYZR4S9

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

D-30308595652700221
D-55308595652700450
D-20308595652700177
D-50308595652700306
D-00308595652700054
D-05308595652700122
D-51308595652700351
D-52308595652700405