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Anterior Cervical Plate
Created with Pixso. Spine Anterior Cervical Plate Titanium Cervical Plate Implant Orthopedic Surgery CE Certification

Spine Anterior Cervical Plate Titanium Cervical Plate Implant Orthopedic Surgery CE Certification

Model Number: Anterior Cervical Plate System
MOQ: 1 pieces
Price: Negotiable
Delivery Time: After receiving the payment, we will send the express within 7 working days
Payment Terms: L/C, T/T
Detail Information
Place of Origin:
China
Certification:
Certification CE / ISO13485:2016
Plate Design:
Low-profile,arc Design
Size:
Various Sizes Available
Plate Length:
22.5mm~110mm
Screw Type:
Self-tapping
OEM:
Avaliable
Classification:
Class III
Warranty:
5 Years
Material:
Titanium
Usage:
Single-use
Shipping:
FEDEX Or Designate
Packaging Details:
Original packaging + carton
Supply Ability:
5,000 pieces per month
Highlight:

Orthopedic Surgery Anterior Cervical Plate

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CE Certification Titanium Cervical Plate

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Orthopedic Surgery cervical fusion plate

Product Description
Quick Detail:
Features of cervical anterior approach plate:
 
*Semi restrictive system, dynamic compression design can promote bone graft fusion.
 
*Low incisions and arc-shaped design, less stimulation to surrounding soft tissues.
 
*The pre bending design conforms to the anatomy, and the application is excellent.
 
*Long groove bone grafting nail hole is convenient for bone grafting.
 
*Large diameter, deep thread screw design, stronger pull-out resistance.
 
*Elastic anti retreat structure, easy to operate.
 
*It has a large window hole, which is convenient for observing the bone graft.
 
*The plum blossom nail head design reduces the possibility of thread slipping.
 
General information: Place of Origin: China
  Type Anterior Cervical Plate System
  Certification CE / ISO13485:2016
MOQ : 1 pieces
Price: Negotiable
Payment Terms: Bank transfer
Supply Ability: 1,0000 pieces per month
Delivery Time: After receiving the payment, we will send the express within 7 working days
Shipping: FEDEX or Designate
Specifications: Length(mm):20,22.5,25,27.5,30,32.5,35,37.5 ( For one-level segment) Length(mm):40,42.5,45,47.5,50,52.5,55 ( For two-level segment) Length(mm):57.5,60,62.5,65,67.5,70,72.5,75 (For three-level segment) Length(mm):77.5,80,82.5,85,87.5,90,95,100,105,110 (For four-level segment) Width(mm):17 Thickness(mm):2
Attentions 1. Please carefully read the instruction before use.
  2. Before the surgery, determine the surgery plan according to the symptom, sign and the image check.
  3. MR examination can be carried out onTi6Al4V product according to routine parameters of the hospital.
  4. Choose the products and special matching tools with suitable specification and model according to the symptom and the position of patients.
  5. Perform the surgery under the directions of an experienced surgeon.
  6. The surgeon shall describe the relevant precautions in details to the patients before the surgery.
  7. At the delivery time, if the product is found scratched, damaged, and bended or cracked, it cannot be used anymore.
  8. The implants and tools provided by our company are not sterilized but the devices must be sterilized before the surgery. We recommend the method of high pressure steaming for sterilization.
  9. Any activities in the early post-operation period, if being conducted improperly in method or extent, would possibly cause the invalidation of the metal implant, such as fixation loosening, broken or bending, etc. For this reason, the time, method and extent of activity in the early post-operation period shall be conducted strictly under the correct instruction of the surgeon, and shall be implemented step by step.
  10. Before healing of bone grafting in early post-operation period, the external fixation shall be used for 6 to 12 weeks.
  11. The product is disposable.
  12. And it is forbidden to be used with products of other materials and model or from other companies.
  13. To avoid contamination, this product should be disposed as infectious medical waste disposal method.
Warning: 1.The products and instruments should be sterilized before use. Recommended to meet the EN ISO 17665-1 related requirements of the high pressure steam sterilization method. Recommended sterilization conditions:Down-draining steam sterilizer: temperature: 121℃; duration of exposure: 30 minutes; barometric pressure: 102.9kPa(1.05kg/cm2); drying time:45 minutes. High pressure steam sterilizer must be approved by the hospital and inspection regularly to ensure the medical device can reach the recommended sterilization temperature during the exposure period.
  2.The product is disposable and should not be reused under any circumstances. Used implants may contain many acquired flaws, or the integrity of itself may be damaged, which will shorten the service life or cause cross infection. Whether
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