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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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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

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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

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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

No registered UDI-DI variants for this device family.