- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 4, 2026
868302007170YHB0790327SJDERMOSEPT - X-LARGE - DERMOSEPT YETİŞKİN HASTA BEZİ-XL is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by ALG İLAÇ SANAYİ TİCARET LTD. ŞTİ.. Placed on the EU market in Türkiye. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08683020071704ALG24-18TR-MF-000045198(01)08683020071704
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 Türkiye; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| TürkiyePrimary placement | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
T04010199INCONTINENCE NAPPIES - 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 →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 →868302007169YHB0760327Z3On the marketDERMOSEPT - MEDIUM - DERMOSEPT YETİŞKİN HASTA BEZİ-M868302007168YHB0780327YSOn the marketDERMOSEPT - SMALL - DERMOSEPT YETİŞKİN HASTA BEZİ-S868302007167YHB0770327XGOn the marketDERMOSEPT 3H CONCENTRATED ENZYMATIC CLEANING SOLUTION FOR MEDICAL INSTRUMENTS AND ENDOSCOPES8683020070271001ENZ11242LOn the marketDERMOSEPT CONCENTRATED INSTRUMENT MAINTENANCE AND CLEANING SOLUTION868302007345KAT1201293GOn the marketDERMOSEPT DT-CONCENTRATED DENTAL CARE AND CLEANING SOLUTION868302007342DT8250129RZOn 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.No certificate specifically references this device's Basic UDI-DI.