- Organization name
- UDI-DI code
- Reference / catalog number
BE-MF-000000257OBA SLA - Long neck - Double hook is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Surgi-Tec NV. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Nov 28, 2025
540700775OBAENPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)05407007750139
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
3 warnings recorded — scroll inside the panel to see all entries.
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 Belgium; available across 11 countries total.
| Country | On market since | Until |
|---|---|---|
| BelgiumPrimary placement | Jan 1, 1999 | Still on market |
| Bulgaria | Aug 27, 2018 | Still on market |
| Cyprus | Nov 10, 2023 | Still on market |
| Germany | Jan 1, 1999 | Still on market |
| EL | Nov 10, 2023 | Still on market |
| Spain | Dec 10, 2013 | Still on market |
| Finland | Mar 28, 2023 | Still on market |
| France | Jan 1, 1999 | Still on market |
| Hungary | May 11, 2017 | Still on market |
| Luxembourg | Jan 1, 1999 | Still on market |
| Netherlands | Jan 1, 1999 | 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.
05407007750139Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
540700775OBAEN02-006SUDI 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.
P01020101DENTAL IMPLANTS540700775OBAENOn the marketOBA Maxilla Pediatric - Short neck - Long hook - Right540700775OBAENOn the marketOBA Maxilla Pediatric - Short neck - Long hook - Right STERILE540700775OBAENOn the marketOBA SLA - Long neck - Double hook STERILE540700775OBAENOn the marketOBA SLA - Short neck - Double hook540700775OBAENOn the marketOBA SLA - Short neck - Double hook STERILE540700775OBAENOn the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
BE24/00000296RestrictedNotified 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.
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