Cryoprobe
- UID
- IMP/MD/2020/000157_33abfa21ad82019fa2431e3f4840c674_16067580cd30acf5b1ee9f123a9e5651
- Device class
- Class D
- Brand name
- Ablation Device
- License holder
- M/S ASIA ACTUAL INDIA (OPC) PVT. LTD.
- Approving authority
- CDSCO
- Product information
- IceCure Cryoablation system is intended for cryogenic destruction of tissue during surgical procedures by the application of extreme cold temperatures. The IceCure Cryoablation system is indicated for use as a cryosurgical tool in the fields of general surgery (Ablation Device), dermatology, thoracic surgery (Ablation Device), gynecology, oncology (Ablation Device), proctology, and urology (Ablation Device). The IceCure Cryoablation system may be used with an ultrasound device to provide real-time visualization of the cryosurgical procedure. The system is suitable for use in a number of cryotherapy applications. However, it is ONLY indicated for use in patients whom the practitioner has deemed eligible for cryotherapy
Cryoprobe is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000157_33abfa21ad82019fa2431e3f4840c674_16067580cd30acf5b1ee9f123a9e5651. This device is marketed under the brand name Ablation Device. The license holder is M/S ASIA ACTUAL INDIA (OPC) PVT. LTD., and it is classified as Device Class Class D. The approving authority is CDSCO.
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.