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.

MICRO APPLICATORS — 20 UDI-DI variants, MDR (Akzenta International SA)

MD Atlas
Akzenta International SA

Data from EUDAMED, last updated May 23, 2026

MICRO APPLICATORS

42504766MICUL

20 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: Akzenta International SA

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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42504766MICUL
Device name: MICRO APPLICATORS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: Akzenta International SA
SRN: CH-MF-000036434
Country: Switzerland
Email: business@akzenta.ch
Phone: +41 (0) 91 921 14 92

Authorised representative

Name: IQX GmbH
SRN: AT-AR-000016713
Country: Austria
Phone: +4369919027671

Variants by status

UDI-DI variants

20 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

basicUdiUlid01KP8V8E1K39WKDFH4TXGPZDN6

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

313686303665318009915
313686203665318009922
313686403665318009908
313686603665318009885
313686503665318009892
PLANDENT400F-P04250476618087
PLANDENT400R-B04250476618094
MICAP25-AKZ-PI-REG04250476618315
MICAP25-AKZ-LI-REG04250476618353
MICAP25-AKZ-BL-REG04250476618339
MICAP25-AKZ-LU-FNE04250476618292
MICAP25-AKZ-MC-FNE04250476618308
MICAP25-AKZ-YE-FNE04250476618377
MICAP25-AKZ-MI-FNE04250476618407
MICAP25-AKZ-WH-SFN04250476618384
MICAP25-AKZ-CE-FNE04250476618285
MICAP25-AKZ-FG-REG04250476618346
PROB00001F04250476624934
PROB00001R04250476624873
PROB00001XF04250476624903