Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

1740/3 — Class IIa MDR by Swissdentacare SA

MD Atlas
Swissdentacare SA

EUDAMED last updated this device on Apr 23, 2026

1740/3

764035775_Proxocare_4R

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Swissdentacare SA
UDI-DI code: 07640357750536
Reference / catalog number: 1740/3

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: Swissdentacare SA
SRN: CH-MF-000016591
Manufacturer status: Active

Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Jul 19, 2019	Still on market

Device identification

Trade name: not provided
UDI-DI code: 07640357750536
Basic UDI-DI: 764035775_Proxocare_4R
Reference / catalog number: 1740/3
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 3
Additional product description: Swissdentacare 1740/3 Proxocare 40 µm Pack of 3 pieces
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q010499ORTHODONTIC DEVICES - OTHER
Q01010199DENTAL RESTORATION DEVICES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

1990/40764035775_G5-Shank_UEOn the market 1990/20764035775_G5-Shank_UEOn the market FS-150/20764035775_G5-Shank_UEOn the market 1300/S2764035775_G5-ProLign_84On the market 1310/5764035775_G5-ProLign_84On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.