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.

starlight-generation-basecap — 33 UDI-DI variants, MDR (ATO FORM GmbH)

MD Atlas
ATO FORM GmbH

Data from EUDAMED, last updated May 23, 2026

starlight-generation-basecap

42511106STLGTGENERATTG

33 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: ATO FORM GmbH

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: 42511106STLGTGENERATTG
Device name: starlight-generation-basecap
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: ATO FORM GmbH
SRN: DE-MF-000008880
Country: Germany
Email: r.friedrich@ato-form.com
Phone: +49 6093 944-266

Variants by status

UDI-DI variants

33 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

basicUdiUlid01KS24Y4YRV61CQY2Q8T6VTQ0J

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

G30000-XXL04251110626994
G20003-S04251110626949
G20001-XXL04251110626918
G20000-S04251110626840
G20003-L04251110626925
G20003-XL04251110626956
G20000-XL04251110626857
G20000-XXL04251110626864
G20000-L04251110626826
G20001-L04251110626871
G30000-XL04251110626987
G30000-M04251110626970
G20001-S04251110626895
G20003-M04251110626932
G20001-XL04251110626901
G20000-M04251110626833
G20003-XXL04251110626963
G20001-M04251110626888
G10001-L04251110626727
G10001-XL04251110626758
G10002-S04251110626796
G10000-XL04251110626703
G10002-XXL04251110626819
G10002-XL04251110626802
G10002-L04251110626772

1 2