Following Warnings should be taken while using the products from Steripharm Ltd FZC

All devices are for single use only.

Do not reuse, reprocess or re-sterilize the medical device.

Devices are supplied sterile. They are sterilized using EO gas.

Do not use if the sterile barrier is damaged. A broken sterile barrier means that the pack is non sterile. Use of non-sterile products may cause infection to the patients.

These products are not intended for permanent use. They are for transient use only.

Count pack components according to the hospital's policy and confirm the contents post-surgery to avoid any complications of material being left behind in the patients. All details of the contents and their quantity are provided on the device labels.

Reuse, reprocessing or re-sterilization may compromise the structural integrity of the pack components and/or lead to device failure which, in turn, may result in patient injury, illness or death.

Reuse, reprocessing or re-sterilization may also create a risk of contamination of the device and/or cause patient infection or cross-infection, including, but not limited to, the transmission of infectious disease(s) from one patient to another. Contamination of the device may lead to injury or serious illness of the patient.

The medical device use should not be carried out by unauthorized and untrained person. The medical device should be used only by well-trained surgeons in support with trained technicians.

Upon completion of procedure dispose of the medical device/pack and its components if any as per institutional and local regulatory guidelines for bio-hazardous medical waste.

Steripharm does not provide any implant/in-dwell components with the packs.

Be careful to avoid injury from sharp instrument points or moving instrument parts.