



[Specification]
Table 1 Specification of Endoscopic Twin Forceps
Model | Effective Length (mm) | Max. Opening Angle |
SS211-2312 | 1200 | ≥90° |
SS211-2314 | 1400 | ≥90° |
SS211-2316 | 1600 | ≥90° |
SS211-2318 | 1800 | ≥90° |
SS211-2323 | 2300 | ≥90° |
Working Channel Diameter of Appropriate Endoscope: Minimum 2.8mm | ||
[Warnings]
1. The device is designed and intended for single use only. DO NOT RESTERILIZE AND/OR REUSE. Reuse or resterilization may 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, illness or death of the patient. Reuse or resterilization may compromise the structural integrity of the device and/or lead to device failure which, in turn, may result in patient injury, illness and death. The manufacturer will not be responsible for any direct, incidental or consequential damages resulting from resterilization or reuse.
2. Please carefully read all instructions prior to use. Failure to observe all warnings and precautions may result in complications.
3. Inspect the product, prior to procedure, to verify functionality and lack of damaged parts. Do not use the product if the outer or the inner package is damaged or opened or if the components appear to be damaged or defective.
4. This device is not intended for use except as indicated in the Intended Use.
5. Only endoscopists thoroughly trained and educated in the performance of the Endoscopic Twin Forceps should use this device.
6. Use before the expiry date.
7. After use, the product may be a potential biohazard. Handle and dispose of in accordance with acceptable medical practice and applicable local, state, and federal laws and regulations related to product contamination by blood.
[Precautions for Use]
1. The product shall be used by endoscopists in medical institutions.
2. This device is intended for single (one) use – only. Do not re-sterilize and/or reuse, as this can potentially result in compromised device performance and increase risk of complications (patient infection, transmission of infectious disease, etc.).
3. If the endoscope cannot be withdrawn with endoscopic forceps, unscrew the screw cap, separate the instrument rod from the handle, remove the handle, and withdraw the endoscope along the rod.
4. When using forceps to access the endoscope, keep the forceps head closed.
CAUTION:Indications, contraindications, warnings and instructions for use can be found in the product IFU supplied with each device. Information for use only in countries with applicable health authority registrations. Products shown for INFORMATION purposes only and may not be approved or for sale in certain countries. Please check availability with your local sales representative or customer service.