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.

SK PODO, SK THERMO, GT PODO, GT SPECIAL — 192 UDI-DI variants, MDR

MD Atlas
LUKAS-ERZETT GmbH & Co.KG

Data from EUDAMED, last updated May 23, 2026

SK PODO, SK THERMO, GT PODO, GT SPECIAL

4027497113115WB

192 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: LUKAS-ERZETT GmbH & Co.KG

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: 4027497113115WB
Device name: SK PODO, SK THERMO, GT PODO, GT SPECIAL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 26, 2024

Manufacturer & authorised representative

Manufacturer

Name: LUKAS-ERZETT GmbH & Co.KG
SRN: DE-MF-000005344
Country: Germany
Email: axel.schmidt@lukas-erzett.de
Phone: 0049 226384250

Variants by status

UDI-DI variants

192 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

basicUdiUlid01HQJD66SAK0P0BYANP6C1EBAP

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

3565804027497237821
A2108010308004027497609444
3565704027497237838
A2108010315004027497609437
A2108010108004027497219766
3562704027497231393
30713007004027497235759
3562904027497231317
A210811208004027497609406
30713006004027497235766
3562804027497231386
A210811215004027497060498
3568404027497230396
A2108013232004027497606443
30713009004027497235681
3566404027497097494
A2108013208004027497600359
30713008004027497235698
A2108013215004027497600366
3567404027497097500
3565304027497237913
A2108013308004027497609420
3565504027497237852
A2108013315004027497609413
3565404027497237890

4 5 6 7 8