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

FP1945 — Class IIa MDD by CF Pharma Ireland Ltd

MD Atlas
CF Pharma Ireland Ltd

EUDAMED last updated this device on Aug 7, 2025

FP1945

B-05907377532576

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: CF Pharma Ireland Ltd
UDI-DI code: 05907377532576
Reference / catalog number: FP1945

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: CF Pharma Ireland Ltd
SRN: IE-MF-000004595
Manufacturer status: Active

Related devices

FP1947B-05391525738017On the market FP1939B-05391525739465On the market Colief Nappy Care SprayB-05014302001547On the market FP1961B-05944702209628On the market FP1963B-05944702209635On 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.

Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement	Aug 7, 2025	Dec 31, 2028

Device identification

Trade name: not provided
UDI-DI code: 05907377532576
Basic UDI-DI: B-05907377532576
Reference / catalog number: FP1945
Issuing entity: GS1

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: Granuskin Face & Body 60ml Hydrogel formulation
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification