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Haemofilter for CRRT - India CDSCO Medical Device Registration

Haemofilter for CRRT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000414_750b20d4de8bf25f53538cfc5f588c75_eaf64469b68d419036900d18627b1fbc. This device is marketed under the brand name Diacap Pro. The license holder is B BRAUN MEDICAL INDIA PRIVATE LIMITED ,OFFICE NO. A/11, GRD FLR, GUNDECHA ONCLAVE PREMISES CHSL, A WING, CTS NO. 99A & 97A, SAKI VILLAGE, KHERANI RD, SAKINAKA, MUMBAI, Tal - SAKINAKA ( MUMBAI-ZONE4 ) ,Mumbai Suburban Maharashtra ,400072 ,India, and it is classified as Device Class Class C. The approving authority is CDSCO.

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CDSCO Registered
Class Class C
Haemofilter for CRRT
UID: IMP/MD/2021/000414_750b20d4de8bf25f53538cfc5f588c75_eaf64469b68d419036900d18627b1fbc

Brand Name

Diacap Pro

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Diacap Acute Haemofilter is indicated for use in patients with fluid overload, uraemia and / or electrolyte disturbances associated with oligoanuric acute renal failure. It may also be used when removal of excess fluid is indicated, such as in patients with pulmonary oedema or congestive heart failure refractory to diuretic therapy.

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