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.

VIADOLFIX — 8 UDI-DI variants, MDR (PRIM, S.A.)

MD Atlas
PRIM, S.A.

Data from EUDAMED, last updated May 23, 2026

VIADOLFIX

843404825MALLATUBULAR59

8 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: PRIM, S.A.

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: 843404825MALLATUBULAR59
Device name: VIADOLFIX
Device model: 70030201
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 7, 2022

Manufacturer & authorised representative

Manufacturer

Name: PRIM, S.A.
SRN: ES-MF-000004651
Country: Spain
Email: eudamed1@prim.es
Phone: + 34 91 334 24 00

Variants by status

UDI-DI variants

8 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

basicUdiUlid01G4D3S4V2C9BFRMZ0Y7G7XCMV

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

7003020108470003285674
7001040108470003285599
7001040208470003285421
7001040308470003285346
7001040408470003285261
7001040508470003285186
7001040608470003285001
7001040708470003284929