Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners 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.

Planmeca ProMax 3D Mid — 2 UDI-DI variants, MDR (Planmeca Oy)

MD Atlas
Planmeca Oy

Data from EUDAMED, last updated May 23, 2026

Planmeca ProMax 3D Mid

6430035420125J

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Planmeca Oy

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?

Device characteristics

Active device

Legacy certificates

Certificate number: FI23/00000059
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: SGS FIMKO OY (0598)
Validity: Sep 17, 2025 → Jun 26, 2030

Identity & classification

Basic UDI-DI: 6430035420125J
Device name: Planmeca ProMax 3D Mid
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jul 3, 2024

Manufacturer & authorised representative

Manufacturer

Name: Planmeca Oy
SRN: FI-MF-000006499
Country: Finland
Email: niina.vuorikallas@planmeca.com

Variants by status

UDI-DI variants

2 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01J1W7G842QBRDSE58P2G06PNH

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

3003858306430035420957
3000311206430035420490