Pure Global
CDSCO UID IMP/MD/2019/000003_ebf5d2138c2100d19465ca5e1245eb84_bb531a4ae0515c50a445c4f530733818

Anchor with Suture

Johnson & Johnson Private Limited·Device Class Class D·India CDSCO·Brand: GII Anchor
Registration details
UID
IMP/MD/2019/000003_ebf5d2138c2100d19465ca5e1245eb84_bb531a4ae0515c50a445c4f530733818
Device class
Class D
Brand name
GII Anchor
License holder
Johnson & Johnson Private Limited
Approving authority
CDSCO
Product information
The GRYPHON Anchor with PROKNOT Technology is intended for: Shoulder: Bankart Repair, SLAP Lesion Repair, Capsular Shift or Capsulolabral Reconstruction Hip: Capsular Repair, Acetabular Labral Repair
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About this record

Anchor with Suture is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000003_ebf5d2138c2100d19465ca5e1245eb84_bb531a4ae0515c50a445c4f530733818. This device is marketed under the brand name GII Anchor. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.

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