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

EFLM-PT-03C-RD-S — Class IIa MDR by Eufoton Srl

MD Atlas
Eufoton Srl

EUDAMED last updated this device on Apr 28, 2026

EFLM-PT-03C-RD-S

805418864FIBRACODCEZ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Eufoton Srl
UDI-DI code: 08054188640680
Reference / catalog number: EFLM-PT-03C-RD-S

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: Eufoton Srl
SRN: IT-MF-000009227
Manufacturer status: Active

Certificates

Certificate health across this manufacturer's portfolio.

ITD 1024592 1Issued
Quality assuranceNotified body: 1936Expiry: May 15, 2029
ITH 1024592 1Issued
Quality management systemNotified body: 1936Expiry: May 15, 2029

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: 08054188640680
Basic UDI-DI: 805418864FIBRACODCEZ
Reference / catalog number: EFLM-PT-03C-RD-S
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 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)08054188640680

Sign in to download the DataMatrix

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

Email

Password

No account yet?

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

Sign in to generate the UDI-PI DataMatrix

Create a free account, then generate the compliant UDI-PI carrier for this device.

Email

Password

No account yet?

EMDN nomenclature code(s)

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

Z12011080LASER SURGERY INSTRUMENTS - HARDWARE ACCESSORIES

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

Related devices

EFLM-DT-015C-S805418864FIBRACODCEZOn the market EFLM-DT-01C-S805418864FIBRACODCEZOn the market EFLM-DT-02C-S805418864FIBRACODCEZOn the market EFLM-DT-03C-S50805418864FIBRACODCEZOn the market EFLM-ELX-025C-RD-S805418864FIBRACODCEZOn the market