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.

BioniQ Instruments — 40 UDI-DI variants, MDR (LASAK s.r.o.)

MD Atlas
LASAK s.r.o.

Data from EUDAMED, last updated May 23, 2026

BioniQ Instruments

85955730002XL

40 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: LASAK s.r.o.

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: 85955730002XL
Device name: BioniQ Instruments
Device model: C-guide for guided surgery; Drill guide for guided drill; Drill stop for drills; Guided fixation pin; Implant carrier remover; Screw remover set; Screw remover set BioniQ; Screwdriver; Screw-On abutment holder
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: LASAK s.r.o.
SRN: CZ-MF-000031907
Country: Czechia
Email: info@lasak.cz

Variants by status

UDI-DI variants

40 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

basicUdiUlid01JXYFFAFVV32FDET79KSJ91EC

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

C-guide for guided surgery, H10 (GS)08595573002138
C-guide for guided surgery, H6 (GS)08595573002145
C-guide for guided surgery, H7.5 (GS)08595573002152
C-guide for guided surgery, H8 (GS)08595573002169
Drill guide for guided drill S2.9 (GS)08595573002190
Drill guide for guided drill S3.5 (GS)08595573002206
Drill guide for guided drill S4.0/T4.0 (GS)08595573002213
Drill guide for guided drill S5.0/T5.0 (GS)08595573002220
Drill stop for drills S2.9, S3.5, S4.0, T4.0 for implants L1008595573000011
Drill stop for drills S2.9, S3.5, S4.0, T4.0 for implants L1208595573000028
Drill stop for drills S2.9, S3.5, S4.0, T4.0 for implants L1408595573000035
Drill stop for drills S2.9, S3.5, S4.0, T4.0 for implants L6.508595573000042
Drill stop for drills S2.9, S3.5, S4.0, T4.0 for implants L808595573000059
Drill stop for drills S5.0, T5.0 for implants L1008595573000066
Drill stop for drills S5.0, T5.0 for implants L1208595573000073
Drill stop for drills S5.0, T5.0 for implants L1408595573000080
Drill stop for drills S5.0, T5.0 for implants L6.508595573000097
Drill stop for drills S5.0, T5.0 for implants L808595573000103
Guided fixation pin – vertical, QN/H10/d5.2 (GS)08595573000127
Guided fixation pin – vertical, QN/H6/d5.2 (GS)08595573000134
Guided fixation pin – vertical, QN/H8/d3.5 (GS)08595573002503
Guided fixation pin – vertical, QN/H8/d5.2 (GS)08595573000141
Guided fixation pin – vertical, QR/H10/d5.2 (GS)08595573000158
Guided fixation pin – vertical, QR/H6/d5.2 (GS)08595573000165
Guided fixation pin – vertical, QR/H8/d5.2 (GS)08595573000172

1 2