Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ 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

Abilar® Nail Fungal Treatment — Class IIa MDD

MD Atlas
Repolar Pharmaceuticals Oy

EUDAMED last updated this device on Apr 28, 2026

Abilar® Nail Fungal Treatment

B-FIMF0000005899010LL

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Repolar Pharmaceuticals Oy
UDI-DI code: D-FIMF0000005899010LL
Reference / catalog number: 9010

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?

Manufacturer information

Organization name: Repolar Pharmaceuticals Oy
SRN: FI-MF-000000589
Manufacturer status: Active

Critical warnings

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

CW083
May cause an allergic reaction (contact dermatitis) when used by people hypersensitive to natural resins (colophony).

Market distribution

Primary placement in Finland; available across 2 countries total.

Country	On market since	Until
FinlandPrimary placement	Dec 1, 2009	May 26, 2024
Sweden	Apr 17, 2020	May 26, 2024

Device identification

Trade name: Abilar® Nail Fungal Treatment
UDI-DI code: D-FIMF0000005899010LL
Basic UDI-DI: B-FIMF0000005899010LL
Reference / catalog number: 9010
Issuing entity: EUDAMED

Classification

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

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://www.repolar.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M0410DRESSINGS FOR NAILS IN THE FORM OF LIQUIDS, GELS AND CREAMS

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

8001B-FIMF0000005898001LCOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.