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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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Plastic Pipettes — 4 UDI-DI variants, MDR (Produits Dentaires SA)

MD Atlas
Produits Dentaires SA

Data from EUDAMED, last updated May 23, 2026

Plastic Pipettes

764015916PIPETTESB4

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: Produits Dentaires SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764015916PIPETTESB4
Device name: Plastic Pipettes
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 12, 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

4 UDI-DI variants

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Applied filters

basicUdiUlid01GPG4G9WNMFDVY68FAPWV58KV

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

1175007640159161608
1175407640159161615
1175707640159161585
1175207640159161578