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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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Swissdentacare G5-ProStrip — 10 UDI-DI variants, MDR

MD Atlas
Swissdentacare SA

Data from EUDAMED, last updated May 23, 2026

Swissdentacare G5-ProStrip

764035775_G5-ProStrip_2G

10 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: Swissdentacare SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764035775_G5-ProStrip_2G
Device name: Swissdentacare G5-ProStrip
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: Swissdentacare SA
SRN: CH-MF-000016591
Country: Switzerland
Email: uh.spiecker@swissdentacare.ch
Phone: +41916045413

Authorised representative

Name: SDC Distribution GmbH
SRN: DE-AR-000014065
Country: Germany
Phone: +41 91 604 54 13

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KKENQ9CBH77K0K70CJV7B4TK

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

1125-1/307640357750123
1100-KIT-NSK-X5507640357750062
1100/S607640357750055
1115/307640357750093
1125/307640357750116
1100/S407640357750048
1115-1/307640357750109
1002-ORTHO-PROSTRIP07640357750031
1140-1/307640357750147
1140/307640357750130