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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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DT8 — 1 UDI-DI variant, MDR (Biotech Dental)

MD Atlas
Biotech Dental

Data from EUDAMED, last updated May 30, 2026

DT8

3701045299981UY

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Biotech Dental

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3701045299981UY
Device name: DT8
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Biotech Dental
SRN: FR-MF-000000669
Country: France
Email: regulatory@biotech-dental.com
Phone: +33(0)4 90 44 60 60

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KSJ44809938N91314X0NMRCZ

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

PKCF0003701045246367