Blood Collection Tube - Sodium Fluoride - India CDSCO Medical Device Registration
Blood Collection Tube - Sodium Fluoride is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000154_0c17cb316514752e429595097604e5f0_1d6243d0d89273e98309541960d08f36. This device is marketed under the brand name KRIVIDA - Vacuum Sodium Heparin. The license holder is GAMMA AGRO-MEDICAL PROCESSINGS PVT.LTD, and it is classified as Device Class Class A. The approving authority is Telangana.
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Brand Name
KRIVIDA - Vacuum Sodium Heparin
License Holder
GAMMA AGRO-MEDICAL PROCESSINGS PVT.LTDDevice Class
Approving Authority
Telangana
Product Information
A sterile plastic tube, sealed with a stopper, containing a pre-measured amount of vacuum, the anticoagulant disodium ethylene diamine tetraacetic acid (KRIVIDA - Vacuum Sodium Heparin) and the antiglycolytic agent sodium fluoride. It is intended to be used for the collection, preservation and/or transport, of blood for analysis and/or other investigation (KRIVIDA - Vacuum Sodium Heparin). This is a single-use device
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Brand: KRIVIDA - Vacuum Sodium Heparin
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Brand: KRIVIDA - Vacuum Sodium Heparin
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Brand: KRIVIDA - Vacuum Sodium Heparin