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.

Offset Reamer Handle — 122 UDI-DI variants, MDR (Incipio Devices SA)

MD Atlas
Incipio Devices SA

Data from EUDAMED, last updated May 23, 2026

Offset Reamer Handle

7630055300502445ORHBT

122 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: 7630055300502445ORHBT
Device name: Offset Reamer Handle
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 23, 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

122 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

basicUdiUlid01K886QJA1WEF7DFZSXXKWNJHM

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

131-174/0507630055306791
S3027007630055305701
90CH.IN.00407630055306722
131-174/0307630055306821
5024450907630055307200
5024450907630055306401
5024450907630055305961
29800107630055305749
803-11-00207630055306944
5024452207630055306005
5024452307630055306425
803-11-00307630055306951
5024452307630055306012
131-174/0107630055306807
5024450407630055307170
5024450407630055307149
5024640407630055307231
5024450407630055306357
01.11.10.087707630055303790
5024450307630055305787
5024452607630055303806
5024452907630055305879
5024451307630055305817
5024453207630055305909
5024451907630055305848

1 2 3 4 5