Pure Global
CDSCO UID MFG/MD/2022/000642_ce674b1bba8784b82995f397200ad63a_509e0f95d7608a0ed7877d31ce011f6b

Bone Nail

GMP Meditech·Device Class Class C·India CDSCO·Brand: Titanium
Registration details
UID
MFG/MD/2022/000642_ce674b1bba8784b82995f397200ad63a_509e0f95d7608a0ed7877d31ce011f6b
Device class
Class C
Brand name
Titanium
License holder
GMP Meditech
Approving authority
Central Drug Standards Control Organization, Ahmedabad
Product information
The Use of Bone Nail provides the orthopaedic surgeon a means of accurate bone fixation and helps generally in the management of fractures and reconstructive surgery. These implants are intended as aids to normal healing but are not intended to replace normal body structures or bear weight of the body in the presence of incomplete bone healing
Similar products (10)
Other products with the same name or brand
Bone Screw
Brand: Titanium
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Bone Screw
Brand: Titanium
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Maxillofacial Implant
Brand: Titanium
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Arthroscopy Implant
Brand: Titanium
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Pins and Wires
Brand: Titanium
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Class C
Spinal Implant
Brand: Titanium
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Bone Plate
Brand: Titanium
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Bone Nail
Brand: SS-Non Sterile
MJ SURGICAL
Class C
Pins & Wires
Brand: Titanium
Universal Orthosystems
Class C
Bone Plates
Brand: Titanium
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Class C
Other products from GMP Meditech
Products from the same license holder (10 products)
Bone Cutter/Punch
Brand: Maxillofacial
Class A
Spinal Cage and Cervical Disk System Instruments
Brand: Maxillofacial
Class A
Plaster Instruments and Saw
Brand: Maxillofacial
Class A
Osteotomes, Chisels & Bone Gouge
Brand: Maxillofacial
Class A
Elevators
Brand: Maxillofacial
Class A
Spinal Instruments
Brand: Maxillofacial
Class A
Cervical and Mesh System Instruments
Brand: Maxillofacial
Class A
Instruments set for Bone Screw and Plates
Brand: Maxillofacial
Class A
Retractor and Extractor
Brand: Maxillofacial
Class A
Wire Tensioner Instruments
Brand: Maxillofacial
Class A
About this record

Bone Nail is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000642_ce674b1bba8784b82995f397200ad63a_509e0f95d7608a0ed7877d31ce011f6b. This device is marketed under the brand name Titanium. The license holder is GMP Meditech, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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