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

ID50-1900 — Class I MDR by I-Dent Innovations for…

MD Atlas
I-Dent Innovations for Dentistry SA

EUDAMED last updated this device on Apr 27, 2026

ID50-1900

++D131ID194R

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: I-Dent Innovations for Dentistry SA
UDI-DI code: +D131ID501900
Reference / catalog number: ID50-1900

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: I-Dent Innovations for Dentistry SA
SRN: CH-MF-000047886
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: +D131ID501900
Basic UDI-DI: ++D131ID194R
Reference / catalog number: ID50-1900
Issuing entity: HIBCC

Classification

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

Device details

Quantity: 1
Additional product description: EverClear 2 - Starter Pack Dental Mirror
Additional information URL: https://www.i-dent-dental.com/ifu
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L160201DENTAL MIRRORS AND HANDLES, REUSABLE

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

ID50-2450++D131ID244JOn the market ID50-2400++D131ID244JOn the market ID50-2070++D131ID194ROn the market ID50-1910++D131ID194ROn the market ID50-1901++D131ID194ROn 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.