U.S. FDA Medical Device Uterine Curette Requirements
FDA Medical Device Definition: An obstetric-gynecologic specialized manual instrument is one of a group of devices used during obstetric-gynecologic procedures to perform manipulative diagnostic and surgical functions (e.g., dilating, grasping, measuring, and scraping), where structural integrity is the chief criterion of device performance. This type of device consists of the following:(1) An amniotome is an instrument used to rupture the fetal membranes.(2) A circumcision clamp is an instrument used to compress the foreskin of the penis during circumcision of a male infant.(3) An umbilical clamp is an instrument used to compress the umbilical cord.(4) A uterine curette is an instrument used to scrape and remove material from the uterus.(5) A fixed-size cervical dilator is any of a series of bougies of various sizes used to dilate the cervical os by stretching the cervix.(6) A uterine elevator is an instrument inserted into the uterus used to lift and manipulate the uterus.(7) A gynecological surgical forceps is an instrument with two blades and handles used to pull, grasp, or compress during gynecological examination.(8) A cervical cone knife is a cutting instrument used to excise and remove tissue from the cervix.(9) A gynecological cerclage needle is a looplike instrument used to suture the cervix.(10) A hook-type contraceptive intrauterine device (IUD) remover is an instrument used to remove an IUD from the uterus.(11) A gynecological fibroid screw is an instrument used to hold onto a fibroid.(12) A uterine sound is an instrument used to determine the depth of the uterus by inserting it into the uterine cavity.(13) A cytological cervical spatula is a blunt instrument used to scrape and remove cytological material from the surface of the cervix or vagina.(14) A gynecological biopsy forceps is an instrument with two blades and handles used for gynecological biopsy procedures.(15) A uterine tenaculum is a hooklike instrument used to seize and hold the cervix or fundus.(16) An internal pelvimeter is an instrument used within the vagina to measure the diameter and capacity of the pelvis.(17) A nonmetal vaginal speculum is a nonmetal instrument used to expose the interior of the vagina.(18) A fiberoptic nonmetal vaginal speculum is a nonmetal instrument, with fiberoptic light, used to expose and illuminate the interior of the vagina.
FDA Uterine Curette Label Requirements and Exceptions
FDA Uterine Curette Import Information
FDA Uterine Curette Detentions (Uterine Curette Entry Refusals)
General U.S. Food and Drug Administration Medical Device Guidelines for:
- Uterine Curette Manufacturers (Uterine Curette Suppliers)
- Uterine Curette Distributors
- Uterine Curette Processors
- Uterine Curette Repackers
- Uterine Curette Relabelers
- Uterine Curette Exporters
- Uterine Curette Importers
For more information about Uterine Curette Medical Devices, simply click below:
U.S. FDA Regulations:
U.S. FDA 510(k) Regulation: 21 C.F.R. section 814.9.
Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.