CDSCO UID MFG/MD/2023/000942_953022009b02f2a1481f4067a7d40fc7_cb196e452b5738e6812a1aa1b86e4db2

Haemodialysis Blood Tubing Set or Haemodialysis Blood Lines Set

Arni Medica Private Limited·Device Class Class B·India CDSCO·Brand: Infusion Set Non-Vented Infuhope
Registration details
UID
MFG/MD/2023/000942_953022009b02f2a1481f4067a7d40fc7_cb196e452b5738e6812a1aa1b86e4db2
Device class
Class B
Brand name
Infusion Set Non-Vented Infuhope
Approving authority
Telangana
Product information
The Blood Tubing Set is intended for acute and chronic Haemodialysis therapy in Kidney dialysis or Nephro failure. Consists of 2 parts: Arterial and Venous line which are used during dialysis with attached fistula and dialyzer. Unique chambers are there which reduce foaming, increase air removal and do not trap EPO (Infusion Set Non-Vented Infuhope). During the Dialysis process the connections between dialyzer equipment and patient is maintained by a medical grade tubing valves called as “Haemodialysis Blood Tubing Set” which consist of different tubing lengths
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Products from the same license holder (8 products)
Transducer Protector
Brand: Infusion Set Non-Vented Infuhope
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Measuring Volume Infusion Set
Brand: Infusion Set Non-Vented Infuhope
Class B
Infusion Set Vented
Brand: Infusion Set Non-Vented Infuhope
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Infusion Set with 0.2 Micron Filter (Infusion Set with 0.2 Micron Filter Infuhope)
Brand: Infusion Set Non-Vented Infuhope
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Micro Infusion Set with Air Vent
Brand: Infusion Set Non-Vented Infuhope
Class B
AV Fistula Needle Set
Brand: Infusion Set Non-Vented Infuhope
Class B
Priming Set
Brand: Infusion Set Non-Vented Infuhope
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Infusion Set Non-Vented
Brand: Infusion Set Non-Vented Infuhope
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About this record

Haemodialysis Blood Tubing Set or Haemodialysis Blood Lines Set is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2023/000942_953022009b02f2a1481f4067a7d40fc7_cb196e452b5738e6812a1aa1b86e4db2. This device is marketed under the brand name Infusion Set Non-Vented Infuhope. The license holder is Arni Medica Private Limited, and it is classified as Device Class Class B. The approving authority is Telangana.

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