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EUDAMED last updated this device on Jul 19, 2026
868213221000DZV1000-T-2 / UNDER KNEE SURGICAL STOCKING OPEN TOE SKIN CCL 2 SIZE 2 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by EFAMED ORTOPEDİ MEDİKAL ÜRÜNLER TİC SAN LTD ŞTİ. Placed on the EU market in Türkiye. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
TR-MF-000031263(01)08682132222011
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 Türkiye; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| TürkiyePrimary placement | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
08682132222011Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
868213221000DZV1000-T-2UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
M030405COMPRESSION STOCKINGSPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →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.868213221000DZOn the marketV1000-S-7 / UNDER KNEE SURGICAL STOCKING OPEN TOE BLACK CCL 2 SIZE 7868213221000DZOn the marketV1000-T-1 / UNDER KNEE SURGICAL STOCKING OPEN TOE SKIN CCL 2 SIZE 1868213221000DZOn the marketV1000-T-3 / UNDER KNEE SURGICAL STOCKING OPEN TOE SKIN CCL 2 SIZE 3868213221000DZOn the marketV1000-T-4 / UNDER KNEE SURGICAL STOCKING OPEN TOE SKIN CCL 2 SIZE 4868213221000DZOn the marketV1000-T-5 / UNDER KNEE SURGICAL STOCKING OPEN TOE SKIN CCL 2 SIZE 5868213221000DZOn the marketNo certificate specifically references this device's Basic UDI-DI.