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

92003075 — Class I MDR by Suomen Hoitolatukku…

MD Atlas
Suomen Hoitolatukku Tuonti Oy

EUDAMED last updated this device on Aug 29, 2022

92003075

6416078FOOTTOEPROTEN

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Suomen Hoitolatukku Tuonti Oy
UDI-DI code: 06416078030759
Reference / catalog number: 92003075

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

92001413M6416078FOOTTOEPROTENOn the market 92001412M6416078FOOTTOEPROTENOn the market 92001401M6416078FOOTTOEPROTENOn the market 92001400M6416078FOOTTOEPROTENOn the market 92001353M6416078FOOTTOEPROTENOn 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.

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

Device identification

Trade name: not provided
UDI-DI code: 06416078030759
Basic UDI-DI: 6416078FOOTTOEPROTEN
Reference / catalog number: 92003075
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: Suojaa ihoa hankaukselta sekä vähentää ihoon kohdistuvaa painetta ja kipua, voi leikata sopivan kokoisen palan.
Additional information URL: https://www.hoitolatukku.fi/
Clinical sizes: 63 x 76 mm

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