Devices (same UDI-DI)
20
Certificates
0
Countries
0
Notified Bodies
0
Basic Information
- Primary DI
- 04260463845181
- Basic UDI-DI Code
- 4260463840018T
- Reference
- 212518
- Device Types
-
Sterilization
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 1
- Status
- On The Market
- Manufacturer
- AKTORmed GmbH
Additional Description
The PROBE PIN is used to register the patient by probing the TROCAR POINT. It is attached to the CANTILEVER instead of the JOINT.
CND Nomenclature Codes
| Code | Description |
|---|---|
| Z1202018099 | REMOTE CONTROL ROBOT-ASSISTED ENDOSCOPIC SURGERY INSTRUMENTS - HARDWARE ACCESSORIES - OTHER |
Related Devices
The Basic UDI-DI associated with this device has 20 devices in total. Below are some other devices sharing the same Basic UDI-DI.
SUPPLY CABLE
Device
EU MDR
·
Eu Md Class 1
·AKTORmed GmbH·On the market
POWER SUPPLY
Device
EU MDR
·
Eu Md Class 1
·AKTORmed GmbH·On the market
STERILISATION TRAY
Device
EU MDR
·
Eu Md Class 1
·AKTORmed GmbH·On the market
ENDOSCOPE CLAMP
Device
EU MDR
·
Eu Md Class 1
·AKTORmed GmbH·On the market
STERILISATION TRAY XL
Device
EU MDR
·
Eu Md Class 1
·AKTORmed GmbH·On the market
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Eu Md Class 1
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·
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EU MDR
·
Eu Md Class 1
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