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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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EndoDrill Drive System — 1 UDI-DI variant, MDR (BiBB Instruments AB)

MD Atlas
BiBB Instruments AB

Data from EUDAMED, last updated May 30, 2026

EndoDrill Drive System

73401799300001PS

1 UDI-DI variant

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

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

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 73401799300001PS
Device name: EndoDrill Drive System
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Sep 17, 2024

Manufacturer & authorised representative

Manufacturer

Name: BiBB Instruments AB
SRN: SE-MF-000008818
Country: Sweden
Email: info@bibbinstruments.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01J7ZFFCDC3S9DZ6PTY3HXNPCE

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

EndoDrill Drive System17340179900078