CDSCO UID IMP/MD/2022/000044_8349a93466860885e74a85ae174ab67e_7634341f9a10b94cc8c6c44e01824b70
Spinal System - Monarch - Connector -Non-Sterile - Titanium
Johnson & Johnson Private Limited·Device Class Class C·India CDSCO·Brand: Non-Sterile
Registration details
- UID
- IMP/MD/2022/000044_8349a93466860885e74a85ae174ab67e_7634341f9a10b94cc8c6c44e01824b70
- Device class
- Class C
- Brand name
- Non-Sterile
- License holder
- Johnson & Johnson Private Limited
- Approving authority
- CDSCO
- Product information
- The ISOLA, VSP, MOSS MIAMI, TIMX and MONARCH Spine Systems are pedicle screw systems intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of the thoracic, lumbar, and sacral spine: degenerative spondylolisthesis with objective evidence of neurological impairment, fracture, dislocation, scoliosis, kyphosis,spinaltumor, and failed previous fusion (Non-Sterile).The ISOLA, VSP, MOSS MIAMI, TIMX and MONARCH Spine Systems are also indicated for pedicle screw fixation for the treatment of severe spondylolisthesis (Non-Sterile) of the L5–S1 vertebra in skeletally mature patients receiving fusion by autogenous bone graft having implants attached to the lumbar and sacral spine (Non-Sterile) with removal of the implants after the attainment of a solid fusion.The ISOLA, MOSS MIAMI, TIMX and MONARCH Spine Systems are also a hook and sacral/iliac screw fixation system of the noncervical spine indicated for degenerative disc disease (Non-Sterile), spondylolisthesis, trauma (Non-Sterile), spinal stenosis, deformities (Non-Sterile),tumor, and previous failed fusion (Non-Sterile).The ISOLA, VSP, and MONARCH Spine Systems when used with pedicle screws are indicated for degenerative disc disease (Non-Sterile). Levels of fixation are for the thoracic, lumbar and sacral spine. The MONARCH Spine System Dual Rod Connectors can be used to connect MONARCH Spine System Rods to rods of other DePuy Spine 4.75mm, 5.5mm, and 6.35mm diameter rod systems
Similar products (10)
Other products with the same name or brand
Fenestrated Screw - Expedium Verse Spinal System - Non -Sterile - Ti/CoCrMo
Brand: Non-Sterile
Johnson & Johnson Private Limited
Class C
Spine System - Rod - Non Sterile
Brand: Non-Sterile
Johnson & Johnson Private Limited
Class C
Expedium Spine System- Spinal System Rod -Non-Sterile -Titanium
Brand: Non-Sterile
Johnson & Johnson Private Limited
Class C
Concorde Spine System Spinal System - Non-Sterile - Polymer Carbon fiber Composite
Brand: Non-Sterile
Johnson & Johnson Private Limited
Class C
Fenestrated Screw System - Non-Sterile -Titanium
Brand: Non-Sterile
Johnson & Johnson Private Limited
Class C
CONFIDENCE Needle -Introducer Needle -Sterile
Brand: Non-Sterile
Johnson & Johnson Private Limited
Class C
Spinal System - Mountaineer OCT - Rod -Non-Sterile -Titanium
Brand: Non-Sterile
Johnson & Johnson Private Limited
Class C
Viper System Spinal System -Screw - Non-Sterile -Titanium
Brand: Non-Sterile
Johnson & Johnson Private Limited
Class C
Fenestrated Screw - Viper Prime Spinal System - Sterile
Brand: Non-Sterile
Johnson & Johnson Private Limited
Class C
CONFIDENCE Kit Spinal Cement System Cement Kit ) -Sterile - PMMA
Brand: Non-Sterile
Johnson & Johnson Private Limited
Class C
Other products from Johnson & Johnson Private Limited
Products from the same license holder (10 products)
C-Section Kit
Brand: PROLENE*
Class D
Coronary Artery Bypass Graft
Brand: PROLENE*
Class D
Coronary Artery Bypass Graft
Brand: PROLENE*
Class D
NON-STERILE NON-ABSORBABLE SURGICAL SUTURE U.S.P.
Brand: BLACK BRAIDED SILK
Class C
Coronary Artery Bypass Graft(ETHICON* CABG KIT)
Brand: PROLENE*
Class D
NON ABSORBABLE SURGICAL SUTURE U. S. P.
Brand: PROLENE*
Class D
NON ABSORBABLE SURGICAL SUTURE U. S. P.
Brand: BLACK BRAIDED SILK
Class C
NON ABSORBABLE SURGICAL SUTURE U. S. P.
Brand: PROLENE*
Class D
ABHY-ADV KIT
Brand: PROLENE*
Class D
Hernia Kit
Brand: PROLENE*
Class D
About this record
Spinal System - Monarch - Connector -Non-Sterile - Titanium is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000044_8349a93466860885e74a85ae174ab67e_7634341f9a10b94cc8c6c44e01824b70. This device is marketed under the brand name Non-Sterile. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class C. The approving authority is CDSCO.
This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.