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

L030NL — Class IIa MDR by Serrix B.V

MD Atlas
Serrix B.V

EUDAMED last updated this device on Mar 13, 2026

L030NL

871830970L0X0EGBT

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Serrix B.V
UDI-DI code: 08718309700959
Reference / catalog number: L030NL

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: Serrix B.V
SRN: NL-MF-000005882
Manufacturer status: Active

Related devices

D060NL871830970D0X0EG8KOn the market M260ES871830970M2X0EGCWOn the market M030ES871830970M0X0EGC8On the market Mycosan Athlete's Foot - 15 mL Brushtube871830970M2X0EGCWOn the market Mycosan Fungal Nail treatment kit - 5mL Brushtube871830970M0X0EGC8On the market

Certificates

Certificate health across this manufacturer's portfolio.

BE23/00000172Supplemented
Quality management systemNotified body: 1639Expiry: Jun 19, 2028

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW275
When pregnant or breastfeeding, only use if instructed by, and under supervision of, a healthcare professional.
CW010
Consult instruction for use (symbol)
CW262
Single patient, multiple use (symbol)

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 Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08718309700959
Basic UDI-DI: 871830970L0X0EGBT
Reference / catalog number: L030NL
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)08718309700959

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.

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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