Catheter Dilator Suppliers
Phone: +45-(47)-192754
Products: Nephrostomy Catheter (FDA Code: LJE), Guidewire Catheter (FDA Code: DQX), Catheter Dilator (FDA Code: GCC), Uterine Manipulator/Injector Cannula (FDA Code: LKF), Diagnostic Biliary Catheter (FDA Code: FGE), Gastro-Urology Catheter & Accessories (FDA Code: KNY), ...
PBN Medicals Denmark A/s offers catheter dilators, guidewire catheters and intrafallopian cannula systems. more...
www.xinhuasurgical.com | Phone: +86-(0533)-3595351
FDA Registration: 3005440795
Products: Vaginal Retractors (FDA Code: HDL), Forceps (FDA Code: HTD), Saws (FDA Code: HSO), Gastroenterologic Needle Holder (FDA Code: FHQ), Self-Retaining Retractors (FDA Code: FFO), Bone Hooks (FDA Code: KIK), ...
Xinhua Surgical Instrument Company Ltd. manufactures surgical instruments. Our products include dental instruments, veterinary instruments, sterilizers, autoclaves and dressing containers, electric su more...
www.sibelsa.be | Phone: 328-145-0459
Products: Wire Twisters (FDA Code: HXS), Automatic Wire Twisters, Surgical Instruments, Wire Twisters, Sternal Wire Twister, Rib Rongeurs (FDA Code: HTX), Disposable Electrosurgical Snare, ...
Simal Sa is a manufacturer of surgical instruments. Our products include micro scissors, tissue forceps, hemostatic forceps, clamping forceps, flat and round handle micro needle holders, bulldog & vas more...
An introduction/drainage catheter is a device that is a flexible single or multilumen tube intended to be used to introduce nondrug fluids into body cavities other than blood vessels, drain fluids from body cavities, or evaluate certain physiologic conditions. Examples include irrigation and drainage catheters, pediatric catheters, peritoneal catheters (including dialysis), and other general surgical catheters. An introduction/drainage catheter accessory is intended to aid in the manipulation of or insertion of the device into the body. Examples of accessories include adaptors, connectors, and catheter needles.
Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to 878.9.
