- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 20, 2025
5903111VAYA-100M3Klin na Haluks z Pierścieniem i Regulacją Twardości S/M 1 zetaw is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by VAYA Spółka z ograniczoną odpowiedzialnością. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
05903111848354VAYA-1035PL-MF-000034726(01)05903111848354
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Poland; available across 1 country total.
Placed on the market in Poland; per-country availability dates not published.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Y061203ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS)Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →5903111METATARSALVNOn the marketKlin na Haluks Vaya SmartGel - L - 1 szt5903111VAYA-100M3On the marketKlin na Haluks Vaya SmartGel - M - 1 szt5903111VAYA-100M3On the marketKlin na Haluks z Pierścieniem i Regulacjąul Tward L/XL 1 zestaw5903111VAYA-100M3On the marketKlin na Haluks z Pierścieniem Vaya SmartGel - L - 1 szt5903111VAYA-100M3On the marketKlin na Haluks z Pierścieniem Vaya SmartGel - M - 1 szt5903111VAYA-100M3On the marketNo 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.No certificate specifically references this device's Basic UDI-DI.