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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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Transparent Strips — 14 UDI-DI variants, MDR (Produits Dentaires SA)

MD Atlas
Produits Dentaires SA

Data from EUDAMED, last updated May 23, 2026

Transparent Strips

764015916TRANSP_STRIPSQC

14 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: Produits Dentaires SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764015916TRANSP_STRIPSQC
Device name: Transparent Strips
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 11, 2023

Manufacturer & authorised representative

Manufacturer

Name: Produits Dentaires SA
SRN: CH-MF-000023147
Country: Switzerland
Email: silvia.contini@pd-dental.com
Phone: +41 21 566 65 07

Authorised representative

Name: PD DENTAL EU SAS
SRN: FR-AR-000017144
Country: France

Variants by status

UDI-DI variants

14 UDI-DI variants

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Applied filters

basicUdiUlid01GPG68DH5XTAZ5KDCQRJEXXCY

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

43713d07640159161905
43711d07640159161875
43712d07640159161882
43703d07640159161868
43701d07640159161844
43702d07640159161851
4202107640159161776
4222207640159161837
4222107640159161790
4221207640159161820
4221107640159161783
4202207640159161813
4201207640159161806
4201107640159161769