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

92003025M — Class I MDR by Suomen Hoitolatukku…

MD Atlas
Suomen Hoitolatukku Tuonti Oy

EUDAMED last updated this device on Jan 13, 2022

92003025M

6416078TOESEP4C

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Suomen Hoitolatukku Tuonti Oy
UDI-DI code: 06416078030254
Reference / catalog number: 92003025M

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: Suomen Hoitolatukku Tuonti Oy
SRN: FI-MF-000011716
Manufacturer status: Active

Related devices

920030756416078FOOTTOEPROTENOn the market 92001413M6416078FOOTTOEPROTENOn the market 92001412M6416078FOOTTOEPROTENOn the market 92001401M6416078FOOTTOEPROTENOn the market 92001400M6416078FOOTTOEPROTENOn 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 Finland; available across 1 country total.

Country	On market since	Until
FinlandPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 06416078030254
Basic UDI-DI: 6416078TOESEP4C
Reference / catalog number: 92003025M
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Korrigerar tåställningen, förhindrar valk.
Additional information URL: https://www.hoitolatukku.fi/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y061203ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS)

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