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.

Smilla — 5 UDI-DI variants, MDR (Schuchmann GmbH & Co. KG)

MD Atlas
Schuchmann GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Smilla

4251040200004000130XXXX8J

5 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: Schuchmann 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: 4251040200004000130XXXX8J
Device name: Smilla
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 20, 2022

Manufacturer & authorised representative

Manufacturer

Name: Schuchmann GmbH & Co. KG
SRN: DE-MF-000013435
Country: Germany
Email: info@schuchmann.de
Phone: +49 5402 407100

Variants by status

UDI-DI variants

5 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

basicUdiUlid01GFJMF6XNFTM973SSWQ4XBZ3M

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

13 00 30004251040200073
13 01 30004251040200097
13 02 20004251040200356
13 00 20004251040200066
13 01 20004251040200080