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.

Transfer Impression — 274 UDI-DI variants, MDR

MD Atlas
APOLLO IMPLANT COMPONENTS SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

Data from EUDAMED, last updated May 31, 2026

Transfer Impression

59043474026RN

274 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: APOLLO IMPLANT COMPONENTS SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

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: 59043474026RN
Device name: Transfer Impression
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: APOLLO IMPLANT COMPONENTS SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ
SRN: PL-MF-000023711
Country: Poland
Email: support@apollocomponents.eu
Phone: +48422252929

Variants by status

UDI-DI variants

274 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

basicUdiUlid01JNK8XW17GK6PR7V4N3FYF9RJ

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

004.2S5.E-054-M4805904890617520
004.2S5.E-022-M4805904890608399
004.2S5.E-044-M4805904890609358
004.2S5.E-019-M4305904890608078
004.2S5.E-056-M5005904890617537
004.2S5.F-056-M5005904890617568
004.2S5.F-018-M4505904890607927
004.2S5.F-006-M4205904890606883
004.2S5.F-044-M4005904890609280
004.2S5.F-044-M4805904890609365
004.2S5.F-054-M4805904890617551
004.2S5.F-031-M4805904890608566
004.2S5.F-019-M4705904890608160
004.2S5.F-012-M4805904890607446
004.2S5.F-019-M4305904890608085
004.2S5.F-016-M4505904890607767
004.2S5.F-053-M4105904890617315
004.2S5.F-022-M4805904890608405
004.2S5.F-010-M5105904890607286
004.2S5.G-044-M4805904890609372
004.2S5.G-010-M5105904890607293
004.2S5.G-012-M4805904890607453
004.2S5.G-019-M4705904890608177
004.2S5.G-031-M4805904890608573
004.2S5.G-018-M4505904890607934