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

800_572 — Class I MDD by Fysioline Oy

MD Atlas
Fysioline Oy

EUDAMED last updated this device on Jan 3, 2022

800_572

B-06418029906151

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Fysioline Oy
UDI-DI code: 06418029906151
Reference / catalog number: 800_572

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: Fysioline Oy
SRN: FI-MF-000001173
Manufacturer status: Active

Related devices

800_546B-84353737087347JOn the market 800_350B-64129889131687JOn the market 704_001B-06418029707000On the market 704_010B-06418029707017On the market 704_0001B-06418029905994On the market

Critical warnings

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

CW011
Avoid contact with eyes, mucous membranes and wounds. Not recommended during pregnancy and nursing. Nor for children under the age of 2. Keep out of the sight and reach of children. Consult your physician if you do not feel better of if you feel worse after 7 days. For external use only.

Market distribution

Primary placement in Finland; available across 1 country total.

Country	On market since	Until
FinlandPrimary placement	Nov 16, 2020	Still on market

Device identification

Trade name: not provided
UDI-DI code: 06418029906151
Basic UDI-DI: B-06418029906151
Reference / catalog number: 800_572
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Cooling cream for the local relief of muscle cramps and muscle soreness. The cream is easily absorbable and provides a pleasant skin feel.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 50 MU24

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

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.