Endometrial curette - India CDSCO Medical Device Registration

Endometrial curette is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000341_f8b09fdddb14b52a07501290fce45f6f_5da21ae88124588de56c9239a05959bc. This device is marketed under the brand name Probet. The license holder is Adhar Healthcare And Devices, and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered

Class Class B

Endometrial curette

UID: IMP/MD/2019/000341_f8b09fdddb14b52a07501290fce45f6f_5da21ae88124588de56c9239a05959bc

Brand Name

Probet

License Holder

Adhar Healthcare And Devices

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Probet is a single-use, sterile, disposable curette for obtaining histological biopsy of the glandular epithelium and superficial chorionic layers of the uterine endometrial wall or sample extraction of uterine menstrual content for any of the following: a) Routine screening for early detection of endometrial carcinoma or other precancerous conditions which could make estrogen therapy inadvisable. b) Evaluation of endometrial tissue response in patients receiving estrogen replacement therapy for menopausal symptoms. c) Endometrial dating and evaluation of uterine pathology associated with infertility, luteal insufficiency, or functional metrorrhagia. d) Identification of specific uterine pathogens by bacterial culturing of uterine samples