- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 27, 2026
5996660Kampo_hor_lapoc8LBone hook, T-handle, angular 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.
05996660022184PF-360-01HU-MF-000006381Primary 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 certificate specifically references this device's Basic UDI-DI.
(01)05996660022184
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 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
L03140199SPREADERS AND RETRACTORS FOR GENERAL SURGERY, REUSABLE - OTHERPrimary 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 →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 →5996660CsontfogokL9On the marketBone holdong forceps, shotrt-beaked, 95 mm5996660CsontfogokL9On the marketBone holging forceps with thread fixation, 170 mm5996660CsontfogokL9On the marketBone lever, 10 mm, 220 mm5996660EmelokYFOn the marketBone lever, 15 mm, 125 mm5996660EmelokYFOn the marketBone lever, 15 mm, 250 mm5996660EmelokYFOn the market