CDSCO UID IMP/MD/2019/000182_3d4356bb7855860b567803347421f189_ac20645bd78f9fc020bd0e96ebbeb456
Haemostat
Johnson & Johnson Private Limited·Device Class Class D·India CDSCO·Brand: CE
Registration details
- UID
- IMP/MD/2019/000182_3d4356bb7855860b567803347421f189_ac20645bd78f9fc020bd0e96ebbeb456
- Device class
- Class D
- Brand name
- CE
- License holder
- Johnson & Johnson Private Limited
- Approving authority
- CDSCO
- Product information
- SURGICEL Powder (CE) is used adjunctively in surgical Procedures to assist in the control of capillary, venous, and small arterial hemorrhage when ligation or other conventional methods of control are impractical or ineffective. SURGICEL Powder can also be applied in laparoscopic or other endoscopic procedures when used with the SURGICEL Endoscopic Applicator.
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About this record
Haemostat is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000182_3d4356bb7855860b567803347421f189_ac20645bd78f9fc020bd0e96ebbeb456. This device is marketed under the brand name CE. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.
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