Pricing Sign in

Role
Country
Date of registration
Address

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.

Organization name
UDI-DI code
Reference / catalog number

DFB-L-M-B12-030 — Class III MDD by ASSUT EUROPE SPA

MD Atlas
ASSUT EUROPE SPA

EUDAMED last updated this device on Feb 27, 2026

DFB-L-M-B12-030

B-58033439173141

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: ASSUT EUROPE SPA
UDI-DI code: 58033439173141
Reference / catalog number: DFB-L-M-B12-030

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?

View device family (Basic UDI)

Manufacturer information

Organization name: ASSUT EUROPE SPA
SRN: IT-MF-000018178
Manufacturer status: Active

Related devices

FR479MAT8033439ASSUFILM-PDOUGOn the market Bioripar - Bovine Pericardium Membrane8033439BIORIPARBOVINOVNOn the market Bioripar - Bovine Pericardium Membrane8033439BIORIPARBOVINOVNOn the market Bioripar - Bovine Pericardium Membrane8033439BIORIPARBOVINOVNOn the market Bioripar - Bovine Pericardium Membrane8033439BIORIPARBOVINOVNOn the market

Certificates

Certificate health across this manufacturer's portfolio.

CSQ0013230524Supplemented
Quality management systemNotified body: 0373Expiry: Aug 7, 2028
CVD003124Issued
Technical documentationNotified body: 0373Expiry: Aug 7, 2028
CVD0030240124Supplemented
Technical documentationNotified body: 0373Expiry: Aug 7, 2028
CVD002023Issued
Technical documentationNotified body: 0373Expiry: Aug 7, 2028
CVD001423Issued
Technical documentationNotified body: 0373Expiry: Aug 7, 2028

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 58033439173141
Basic UDI-DI: B-58033439173141
Reference / catalog number: DFB-L-M-B12-030
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)58033439173141

Sign in to download the DataMatrix

Create a free account to download the UDI-DI DataMatrix for this device.

Email

Password

No account yet?

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

H0199SURGICAL SUTURES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Become a partner of MD Atlas