Sharp Head Reduction (Forceps Upper Limbs)

Organization name

SRN

CN-MF-000004851

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• CW999

  -To minimize the risk of infection, these devices must be cleaned and sterilized prior to the first use and after every subsequent use. -Assembled instruments will not clean or sterilize completely. Disassemble all instruments prior to cleaning and sterilization. -Using unspecified sterilization cycles or agents may damage the device or result in incomplete sterilization. -Wear appropriate protective equipment: gloves, eye protection, etc. -Clinical orthopedics with the qualification of vice-director physician or above (including vice-director physician) can use this product and give detailed medical advice to patients. -The products may be used in conjunction with other implants and supporting surgical instruments. The products from different manufactures should never be used together. -If tool wear or defect affects normal use, it should be prohibited.

Primary placement in Netherlands; available across 1 country total.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• L091399ORTHOPAEDIC SURGERY FORCEPS, REUSABLE - OTHER

• Class I medical devices in EUDAMED

No certificate specifically references this device's Basic UDI-DI.