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.

EUS-Needles — 6 UDI-DI variants, MDR (FUJIFILM medwork GmbH)

MD Atlas
FUJIFILM medwork GmbH

Data from EUDAMED, last updated May 23, 2026

EUS-Needles

4044503017813S

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: FUJIFILM medwork 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

Legacy certificates

Certificate number: 1000297126
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: DQS Medizinprodukte GmbH (0297)
Validity: Jan 29, 2026 → Oct 1, 2028

Identity & classification

Basic UDI-DI: 4044503017813S
Device name: EUS-Needles
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: FUJIFILM medwork GmbH
SRN: DE-MF-000008444
Country: Germany
Email: info_ffmw@fujifilm.com
Phone: +49 91 93 500 900

Variants by status

UDI-DI variants

6 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

basicUdiUlid01KEEC4AZYFKXJCQAGH1ADPWM8

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

7010017141204044503017826
7010017141504044503017833
7010017141104044503017840
7010017141304044503017857
7010017141404044503017864
7010017141004044503017871