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EUDAMED last updated this device on May 11, 2026
8682678537KSKQ23 ml Şurup Kaşığı( Tırnaklı ) is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by SENPA PLASTİK SANAYİ VE TİCARET ANONİM ŞİRKETİ . Placed on the EU market in Türkiye. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08682678537075I0014(01)08682678537075
European Medical Device Nomenclature — the EU product classification assigned to this device.
V0399MEASUREMENT DEVICES - OTHERTR-MF-0000343592975-MED-2501601The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Türkiye; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| TürkiyePrimary placement | — | Still on market |
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.
View in glossary →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.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
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 →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 →8682678537KDHNFOn the market23 ml Dosage Cup8682678537KDHNFOn the market23 ml Dosage Cup8682678537KDHNFOn the market3 ml’lik Şurup Kaşığı Toplu8682678537KSKQ2On the market3 ml’lik Topsuz Şurup Kaşığı Kristal8682678537KSKQ2On the market3 ml’lik Topsuz Şurup Kaşığı Moblen8682678537KSKQ2On the marketCertificate health across this manufacturer's portfolio.
2975-MED-2501601IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →