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.

FILBLOC — 885 UDI-DI variants, MDR (ASSUT EUROPE SPA)

MD Atlas
ASSUT EUROPE SPA

Data from EUDAMED, last updated May 30, 2026

FILBLOC

8033439FILBLOCPDOV7

885 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Manufacturer: ASSUT EUROPE SPA

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

Implantable

Legacy certificates

Certificate number: CSQ0013230524
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: ISTITUTO SUPERIORE DI SANITA' (0373)
Validity: Aug 6, 2024 → Aug 7, 2028

Certificate number: CVD001423
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: ISTITUTO SUPERIORE DI SANITA' (0373)
Validity: Aug 8, 2023 → Aug 7, 2028

Identity & classification

Basic UDI-DI: 8033439FILBLOCPDOV7
Device name: FILBLOC
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: Nov 6, 2024

Manufacturer & authorised representative

Manufacturer

Name: ASSUT EUROPE SPA
SRN: IT-MF-000018178
Country: Italy
Email: v.dicintio@assuteurope.com
Phone: +39 0863 515000

Variants by status

UDI-DI variants

885 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

basicUdiUlid01JC0KXQPZK3QVHCJQHXG509RK

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

FS412HHAB18033439388288
FS797KHAH18033439387519
FU99EHHWAS18033439397716
FV373HHAB18033439399208
FU799KHAH18033439392100
FU850HHAH18033439393947
FQ701HHAC18033439383757
FV68CHHAB18033439397952
FU978HHAB18033439395361
FS17CHHAD18033439387939
FU246HHST18033439393725
FU978KHHAX18033439393169
FV386HHAH18033439397440
FS412HHAD18033439388301
FU530KHAE18033439393152
FS979KHAF18033439389629
FS797HHAB18033439390328
FU066KHAF18033439396665
FU429KHAB18033439392025
FU15CKHHAC18033439392087
FR173KHAP18033439384280
FV386HHAB18033439397624
FR249HHAD18033439384679
FU400HAE18033439396535
FQ05AHHAH18033439382903