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

FV373HHAA18033439396894
FR801KHAI18033439386505
FR574HHAB18033439385898
FP33AHHAM18033439382682
FU24BHHWSC18033439392452
FS464HHAB18033439389391
FV386HHAE18033439398539
FQ07GHHAE18033439383085
FV13BKHHAC18033439398171
FR22CHHAB18033439384358
FQ07EHHAP18033439382972
FS565KHWAE18033439389711
FP214HHAB18033439382569
FU978KHAF18033439391493
FQ07GKHAH18033439383115
FU363HHAB18033439393404
FU429HHAB18033439392889
FS979KHHAF18033439387328
FU871KHWAA18033439392643
FS02GHWAM18033439389490
FR26AHNBQ18033439384723
FV373KHAC18033439396931
FS129KHAC18033439387748
FU564HHWAD18033439395064
FU38EHWAH18033439394333