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EUDAMED last updated this device on Dec 8, 2023
B-B961DP786157270ATRAUMATIC MICRO FORCEPS ANGLED, 180 MM - 7" is an MDD-legacy medical device registered in EUDAMED. It is classified as Class I. Manufactured by Daddy D Pro. Placed on the EU market in Portugal. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
B961DP786157270DP-786-15-727 PK-MF-000035172B961DP786157270
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA / IFA support is coming.
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 Portugal; available across 4 countries total.
| Country | On market since | Until |
|---|---|---|
| PortugalPrimary placement | — | Still on market |
| Germany | — | Still on market |
| Spain | — | Still on market |
| Poland | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
L031306HEMOSTATIC FORCEPS, 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.++B961DDPD226MXOn the marketATRAUMATIC MICRO FORCEPS ANGLED, 150 MM - 6" X = 2.0MMB-B961DP786157300On the marketATRAUMATIC MICRO FORCEPS ANGLED, 150 MM - 9"B-B961DP786157290On the marketATRAUMATIC MICRO FORCEPS ANGLED, 180 MM - 7" X = 2.0MMB-B961DP786157310On the marketATRAUMATIC MICRO FORCEPS ANGLED, 210 MM - 8¼"B-B961DP786157280On the marketATRAUMATIC MICRO FORCEPS STRAIGHT, 150 MM - 6"B-B961DP786157180On the marketNo certificate specifically references this device's Basic UDI-DI.