Pure Global

Abortion suction system manual aspirator - India CDSCO Medical Device Registration

Abortion suction system manual aspirator is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2018/000086_f08f5b7c5d54dda4485c23697f3b439a_be1fd0ab72644bd7ff17853c2c9b5615. This device is marketed under the brand name Foley Balloon Catheter 100 % Silicone-2 Way. The license holder is Sterimed Medical Devices Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Haryana.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
Abortion suction system manual aspirator
UID: MFG/MD/2018/000086_f08f5b7c5d54dda4485c23697f3b439a_be1fd0ab72644bd7ff17853c2c9b5615

Brand Name

Foley Balloon Catheter 100 % Silicone-2 Way

Device Class

Class B

Approving Authority

Haryana

Product Information

A Non-Sterile, Manual, Syringe-like Device to aspirate fluid from the uterus for treatment of incomplete abortion, first trimester abortion, and/or for menstrual regulation. Also used for endometrial biopsy

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing