Pure Global
CDSCO UID IMP/MD/2020/000141_710fdb6adb881b408116ef95335e1961_b6a4e6972068c54c7ad816e7afcfdd45

Mesh

Johnson & Johnson Private Limited·Device Class Class D·India CDSCO·Brand: Proceed Ventral Patch
Registration details
UID
IMP/MD/2020/000141_710fdb6adb881b408116ef95335e1961_b6a4e6972068c54c7ad816e7afcfdd45
Device class
Class D
Brand name
Proceed Ventral Patch
License holder
Johnson & Johnson Private Limited
Approving authority
CDSCO
Product information
ULTRAPRO ADVANCED™ Mesh is indicated for the repair of abdominal wall hernias and abdominal wall deficiencies that require the addition of a reinforcing material to obtain the desired surgical result
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About this record

Mesh is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000141_710fdb6adb881b408116ef95335e1961_b6a4e6972068c54c7ad816e7afcfdd45. This device is marketed under the brand name Proceed Ventral Patch. 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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