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.

Alkalický promývací roztok — 24 UDI-DI variants, IVDR (SKALAB s.r.o.)

MD Atlas
SKALAB s.r.o.

Data from EUDAMED, last updated May 23, 2026

Alkalický promývací roztok

859421408SKAIVDP4

24 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: SKALAB 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

Companion diagnostics

Identity & classification

Basic UDI-DI: 859421408SKAIVDP4
Device name: Alkalický promývací roztok
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Feb 2, 2026

Manufacturer & authorised representative

Manufacturer

Name: SKALAB s.r.o.
SRN: CZ-MF-000029744
Country: Czechia
Email: skalab@skalab.cz
Phone: +420777176107

Variants by status

UDI-DI variants

24 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

basicUdiUlid01KGEYDS15CHYZTD130TJDFADZ

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

P 413.0108594214080023
20608594214080016
08-118432 G808594214080047
08-11843208594214080030
P 012.02.M08594214080184
P 012.02.Z08594214080177
P 213.0208594214080054
P 213.02.Z08594214080221
P 123.0208594214080238
P 123.02.Z08594214080245
106-001688-9908594214080207
B 01-4171-5808594214080061
P 109.0108594214080078
P 114.50008594214080085
P 313.0108594214080092
B 01-4179-5208594214080108
P 313.10008594214080115
P 115.50008594214080252
P 115.60008594214080122
YRE B 01-4178-0108594214080139
0030343.00108594214080153
209.900.01108594214080191
P 012.0108594214080146
P 012.0508594214080214