Cryoprobe - India CDSCO Medical Device Registration

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.

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CDSCO Registered

Class Class D

Cryoprobe

UID: IMP/MD/2020/000157_33abfa21ad82019fa2431e3f4840c674_16067580cd30acf5b1ee9f123a9e5651

Brand Name

Ablation Device

License Holder

M/S ASIA ACTUAL INDIA (OPC) PVT. LTD.

Device Class

Class D

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