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.

MIM Acetabular Reamer — 42 UDI-DI variants, MDR (Incipio Devices SA)

MD Atlas
Incipio Devices SA

Data from EUDAMED, last updated May 23, 2026

MIM Acetabular Reamer

7630055300501410REA7Y

42 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Incipio Devices 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

Reusable

Identity & classification

Basic UDI-DI: 7630055300501410REA7Y
Device name: MIM Acetabular Reamer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: Incipio Devices SA
SRN: CH-MF-000030518
Country: Switzerland
Email: surveillance@incipiodevices.ch
Phone: +41 32 754 34 34

Authorised representative

Name: MDSS GmbH
SRN: DE-AR-000005430
Country: Germany

Variants by status

UDI-DI variants

42 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

basicUdiUlid01KAGAN1JQN18J10T1VPF5MGNB

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

5014106507630055305541
5014106607630055305558
5014106707630055305565
5014106807630055305572
370050220668507630055307262
370050220669207630055307279
370050220670807630055307286
370050220671507630055307293
370050220672207630055307309
370050220673907630055307316
370050220674607630055307323
370050220675307630055307330
370050220676007630055307347
370050220677707630055307354
370050220678407630055307361
370050220679107630055307378
370050220680707630055307385

1 2