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EUDAMED last updated this device on Sep 26, 2025
896110404PLIERCLASSI7QSCREW TECH BRACKET REMOVING PLIER WITH PLASTIC TIP , 13CM is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Mark One Surgical. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08961104040007D-035-022PK-MF-000031202(01)08961104040007
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
1 warning recorded — scroll inside the panel to see all entries.
CW010Sterile
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 Spain; available across 1 country total.
Placed on the market in Spain; per-country availability dates not published.
European Medical Device Nomenclature — the EU product classification assigned to this device.
L150702ORTHODONTIC PLIERS, 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 →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 →No 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.896110404RUBERINSCLASSI3BOn the marketRUBBER DAM PUNCH896110404RUBERINSCLASSI3BOn the marketRUBBER DAM TAMPLATE896110404RUBERINSCLASSI3BOn the marketSEPARATORS PLACING PLIER 15.5CM STR896110404PLIERCLASSI7QOn the marketSET OF 10 IMPRESSION TRAYS PERFORATED896110404IMP/TAYCLASSIUTOn the marketSET OF 10 IMPRESSION TRAYS SOLID896110404IMP/TAYCLASSIUTOn the marketNo certificate specifically references this device's Basic UDI-DI.