CDSCO UID MFG/MD/2020/000012_dfef37572cef97239ab7478e3776f04e_267b82dfbcc06cdf3c19fd033c250676

Coronary Artery Bypass Graft(ETHICON* CABG KIT)

Name: Coronary Artery Bypass Graft(ETHICON* CABG KIT) — CDSCO UID MFG/MD/2020/000012_dfef37572cef97239ab7478e3776f04e_267b82dfbcc06cdf3c19fd033c250676
Creator: Johnson & Johnson Private Limited
Keywords: Coronary Artery Bypass Graft(ETHICON* CABG KIT), MFG/MD/2020/000012_dfef37572cef97239ab7478e3776f04e_267b82dfbcc06cdf3c19fd033c250676, PROLENE*, Device Class Class D, Johnson & Johnson Private Limited, CDSCO registration

Johnson & Johnson Private LimitedDevice Class Class DIndia CDSCOBrand: PROLENE*

VerifiedCDSCO · official registry

Registration details

UID: MFG/MD/2020/000012_dfef37572cef97239ab7478e3776f04e_267b82dfbcc06cdf3c19fd033c250676
Device class: Class D
Brand name: PROLENE*
License holder: Johnson & Johnson Private Limited
Approving authority: Central Drug Standards Control Organization, West Zone
Product information: Surgical Procedures related to Coronary Artery Bypass.

About this record

Coronary Artery Bypass Graft(ETHICON* CABG KIT) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000012_dfef37572cef97239ab7478e3776f04e_267b82dfbcc06cdf3c19fd033c250676. This device is marketed under the brand name PROLENE*. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West Zone.

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