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

Matti_001 — Class I MDD by Creative Therapy

MD Atlas
Creative Therapy

EUDAMED last updated this device on Apr 24, 2024

Matti_001

B-MATTI_001SV

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Creative Therapy
UDI-DI code: D-MATTI_001SV
Reference / catalog number: Matti_001

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: Creative Therapy
SRN: BE-MF-000000575
Manufacturer status: Active

Market distribution

Primary placement in Belgium; available across 1 country total.

Placed on the market in Belgium; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: D-MATTI_001SV
Basic UDI-DI: B-MATTI_001SV
Reference / catalog number: Matti_001
Issuing entity: EUDAMED

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: Matti is an interactive rehabilitation tool. Matti will be used during rehabilitation / prevention exercises.With Matti we aim to increase motivation during rehabilitation.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 1900–2000 MU82

EMDN nomenclature code(s)

Z12069082VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - SOFTWARE ACCESSORIES
Z12069080VARIOUS PHYSIOTHERAPY AND REHABILITATION 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

Squeezi 1.0 Handheld device (EN)5430002891SQZ55131314UXOn 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.