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

004.1S10.B-019-M4705904890608122
004.1S10.B-018-M4505904890607880
004.1S10.B-031-M4805904890608528
004.1S10.B-053-M4105904890617278
004.1S10.B-019-M4305904890608047
004.1S10.B-044-M4805904890609327
004.1S10.B-006-M4205904890606845
004.1S10.B-022-M4805904890608368
004.1S10.B-044-M4005904890609242
004.1S10.B-010-M5105904890607248
004.1S10.C-056-M5005904890617476
004.1S10.C-031-M4805904890608535
004.1S10.C-018-M4505904890607897
004.1S10.C-006-M4205904890606852
004.1S10.C-044-M4805904890609334
004.1S10.C-044-M4005904890609259
004.1S10.C-016-M4505904890607736
004.1S10.C-019-M4705904890608139
004.1S10.C-022-M4805904890608375
004.1S10.C-053-M5005904890604896
004.1S10.C-010-M5105904890607255
004.1S10.C-019-M4305904890608054
004.1S10.C-054-M4805904890617469
004.1S10.C-053-M4105904890617285
004.1S10.C-012-M4805904890607415