Mesh - India CDSCO Medical Device Registration

Mesh is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000141_710fdb6adb881b408116ef95335e1961_891625c96d38342aa04571bde85eeae4. 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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CDSCO Registered

Class Class D

Mesh

UID: IMP/MD/2020/000141_710fdb6adb881b408116ef95335e1961_891625c96d38342aa04571bde85eeae4

Brand Name

Proceed Ventral Patch

License Holder

Johnson & Johnson Private Limited

Device Class

Class D

Approving Authority

CDSCO

Product Information

ULTRAPRO™ 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