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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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Silasto® — 4 UDI-DI variants, MDR

MD Atlas
Dr. Hinz Dental-Vertriebsgesellschaft mbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Silasto®

4260620320084X

4 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: Dr. Hinz Dental-Vertriebsgesellschaft mbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4260620320084X
Device name: Silasto®
Device model: Silasto®
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 31, 2024

Manufacturer & authorised representative

Manufacturer

Name: Dr. Hinz Dental-Vertriebsgesellschaft mbH & Co. KG
SRN: DE-MF-000006965
Country: Germany
Email: info@dr-hinz-dental.de
Phone: 00492323593420

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01HNFK00ZHZM78JVS3XG1K28WN

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

Silasto 7004260620321008
Silasto® 3004260620320988
Silasto® 5004260620320995
Silasto® polishing-fluid04260620320667