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EUDAMED last updated this device on May 27, 2026
5996660Csipeszek7JAdson's delicate forceps, 150 mm, 1x2 teeth is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by SUBAN Kéziműszer Hungary Zártkörűen Működő Részvénytársaság. Placed on the EU market in Hungary. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
HU-MF-000006381(01)05996660011096
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 Hungary; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| HungaryPrimary 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.
05996660011096Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
5996660Csipeszek7JPC-092-15UDI 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.
L031308SURGICAL AND ANATOMICAL TWEEZERS, REUSABLEPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Certificate health across this manufacturer's portfolio.
25 0316 QA/NBIssuedNotified 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 →No certificate specifically references this device's Basic UDI-DI.
5996660Csipok3AOn the marketAdson's bone rongeur, 3x4 teeth, narrow, 210 mm5996660Csipok3AOn the marketAdson's delicate forceps, 120 mm, 1x2 teeth5996660Csipeszek7JOn the marketAdson's delicate forceps, 180 mm, 1x2 teeth5996660Csipeszek7JOn the marketAdson's dressing forceps, curved, 120 mm5996660Csipeszek7JOn the marketAdson's dressing forceps, straight, 120 mm5996660Csipeszek7JOn the market