CDSCO UID MFG/MD/2022/000648_1f854ef6f7a24d677837208d59963972_f1941a18bf791653366c0a60b4b6c268

Sterile Latex Free Gloves Surgical Gloves Powder-free

MRK HEALTHCARE PRIVATE LIMITED·Device Class Class B·India CDSCO·Brand: NULIFE, NUFIT, NUFLOW, MEDI-AID, NURAZ, KINGS, SUPERB, DEN-V, DIVINECARE, PREMIERCARE, TOPCARE, NEWMED, STARGLOVE, SFM, GSB, DV FRIENDS, SKRILL, NOVASOFT, FELMEDICA, BENESIT, PROTEX
Registration details
UID
MFG/MD/2022/000648_1f854ef6f7a24d677837208d59963972_f1941a18bf791653366c0a60b4b6c268
Device class
Class B
Brand name
NULIFE, NUFIT, NUFLOW, MEDI-AID, NURAZ, KINGS, SUPERB, DEN-V, DIVINECARE, PREMIERCARE, TOPCARE, NEWMED, STARGLOVE, SFM, GSB, DV FRIENDS, SKRILL, NOVASOFT, FELMEDICA, BENESIT, PROTEX
Approving authority
Kokan Division
Product information
To reduce the risk of contamination of health-care workers hands with blood and other body fluids. To reduce the risk of germ dissemination to the environment and of transmission from the health-care worker to the patient and vice versa, as well as from one patient to another
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Sterile Surgical Latex Gloves Powder Free
Brand: NULIFE, NUFIT, NUFLOW, MEDI-AID, NURAZ, KINGS, SUPERB, DEN-V, DIVINECARE, PREMIERCARE, TOPCARE, NEWMED, STARGLOVE, SFM, GSB, DV FRIENDS, SKRILL, NOVASOFT, FELMEDICA, BENESIT, PROTEX
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Brand: NULIFE, NUFIT, NUFLOW, MEDI-AID, NURAZ, KINGS, SUPERB, DEN-V, DIVINECARE, PREMIERCARE, TOPCARE, NEWMED, STARGLOVE, SFM, GSB, DV FRIENDS, SKRILL, NOVASOFT, FELMEDICA, BENESIT, PROTEX
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About this record

Sterile Latex Free Gloves Surgical Gloves Powder-free is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000648_1f854ef6f7a24d677837208d59963972_f1941a18bf791653366c0a60b4b6c268. This device is marketed under the brand name NULIFE, NUFIT, NUFLOW, MEDI-AID, NURAZ, KINGS, SUPERB, DEN-V, DIVINECARE, PREMIERCARE, TOPCARE, NEWMED, STARGLOVE, SFM, GSB, DV FRIENDS, SKRILL, NOVASOFT, FELMEDICA, BENESIT, PROTEX. The license holder is MRK HEALTHCARE PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is Kokan Division.

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