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

6094 — Class III MDR by Diaco Biofarmaceutici srl

MD Atlas
Diaco Biofarmaceutici srl

EUDAMED last updated this device on Feb 27, 2026

6094

805902020FILLERHC4

On the marketClass III

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Diaco Biofarmaceutici srl
UDI-DI code: 08059020201456
Reference / catalog number: 6094

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: Diaco Biofarmaceutici srl
SRN: IT-MF-000012117
Manufacturer status: Active

Related devices

6097805902020FILLERHC4On the market 6095805902020FILLERHC4On the market 6093805902020FILLERHC4On the market 6053805902020FILLERHC4On the market 6098805902020FILLERHC4On the market

Certificates

Certificate health across this manufacturer's portfolio.

CVD005326Issued
Technical documentationNotified body: 0373Expiry: Feb 11, 2031
CVD005226Issued
Technical documentationNotified body: 0373Expiry: Feb 11, 2031
CSQ0033260126Supplemented
Quality management systemNotified body: 0373Expiry: Feb 11, 2031

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: 08059020201456
Basic UDI-DI: 805902020FILLERHC4
Reference / catalog number: 6094
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: con 2 aghi 22G x 1½" (0.7 x 40 mm) (Becton Dickinson S.A., Spain)
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 2 MU48
1.1 MU01

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

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

P900402RESORBABLE FILLING AND RECONSTRUCTION DEVICES

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