【Product Name】
Ureteral Stent
【Applicable Model】
US-4.8F-1、US-6F-1、US-7F-1、US-4.8F-2、US-6F-2、US-7F-2
【Registrant/Information of manufacturer】
Registrant/Manufacturer/After-sales service:
ANHUI AEROSPACE BIOTECHNOLOGY CO.,LTD.
Domicile : Comprehensive Workshop 1, No. 1319 Shanxiang Road, Bengbu City, Anhui Province
Manufacturer Address: No.1319 Shanxiang
Road,High-tech Zone ,Bengbu City
Manufacturer License Number:Anhui Drug Administration Production License NO. 20150011
Registration Number/Product Specification Number:
MPA.AH Certified No.20202140445
TEL:+86-400-0552-689
【Product Performance】
The flow of ureteral stent should not be less than 3mL/min.
The product should be sterile.
The residual amount of Ethylene Oxide should be less than 10 μ g/g。
The distal of ureteral stent shall be X-ray impervious.
|
Model |
Stent Diameter |
Stent Length |
|
US-4.8F-1 US-4.8F-2 |
1.58 mm |
260mm |
|
US-6F-1 US-6F-2 |
2.00 mm |
260mm |
|
US-7F-1 US-7F-2 |
2.33 mm |
260mm |
【Main structure or composition】
It consists of ureteral stent and push tube. The ureteral stent is made of polyurethane (PU), and the push tube is made of polypropylene (PP).
After sterilization with Ethylene Oxide, the product should be sterile.
【Scope of application】
It is placed between the kidney and bladder to support and drain the human ureter.
【Contraindications】
It is forbidden for patients with abnormal obstruction of ureter, cystitis and severe urinary tract infection.
