- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 15, 2026
B-08680400436726BİOLAS Endosealer 20-(Cerrahi Yapıştırıcı 1cc) is an MDD-legacy medical device registered in EUDAMED. It is classified as Class III. Manufactured by FG GRUP SAĞLIK İNŞAAT HARİTA MİMARLIK MÜHENDİSLİK ELEKTRONİK SANAYİ VE TİCARET ANONİM ŞİRKETİ. Placed on the EU market in Türkiye. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
TR-MF-000027182M.2013.106.2573-1M.2013.106.2573-1(01)08680400436726
4 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 Türkiye; available across 3 countries total.
| Country | On market since | Until |
|---|---|---|
| TürkiyePrimary placement | — | Still on market |
| Spain | — | Still on market |
| Italy | — | 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.
08680400436726Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-08680400436726CA0119UDI 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.
H90010102SYNTHETIC GLUESPrimary 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.
B-08680400437020On the marketBIOLAS Embolizan ajan uygulama kateteri birlikte set VIB-08680400437037On the marketBIOLAS Endosealer 100-( Cerrahi Yapıştırıcı 2cc)B-08680400433039On the marketBIOLAS Endosealer 40-(Cerrahi Yapıştırıcı 2cc)B-08680400436733On the marketBIOLAS Endosealer 80-(Cerrahi Yapıştırıcı 1cc)B-08680400433022On the marketBIOLAS Endoselaer 60-(Cerrahi Yapıştırıcı 3cc)B-08680400436740On the marketNo 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.