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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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Dental manual instruments non invasive — 2 UDI-DI variants, MDR

MD Atlas
Deppeler SA

Data from EUDAMED, last updated May 23, 2026

Dental manual instruments non invasive

764038077CL1K9

2 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: Deppeler SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764038077CL1K9
Device name: Dental manual instruments non invasive
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 27, 2022

Manufacturer & authorised representative

Manufacturer

Name: Deppeler SA
SRN: CH-MF-000019312
Country: Switzerland
Email: info@deppeler.ch

Authorised representative

Name: Swiss Dental Europe SASU
SRN: FR-AR-000016511
Country: France

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FZD7G8CYSH8K4QSTSCFNDQ5W

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

08BR0607640380770020
DMS07640380773243