TRUTACK Hernia Fixation Device TRUTACK Hernia FixationTRUTACK Hernia Fixation DeviceM30)

ITC-HSN: 90189099

408.09 / Piece

Min Order Qty 1 Piece

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Product Description Hernia Fixation Device
Purpose For fixation of mesh during hernia procedure
PRODUCT INFORMATION
Fixation material Non Absorbable material
Type of fixation Single Point
Material of Tack/Glue Titanium
Mode of Firing for device Manual
Duration of Absorbtion NA in case of Non Absorbable
MRI Compatibility Yes
Number of Fasteners/Hooks 30
Length of Fasteners/Hooks (±0.5 mm) 3 mm to 5 mm
The fixation device shall have indicator regarding usage of fasteners/hooks and remaining tackers Yes
Length of the fixation canulla of device in Centimeter (±0.5 mm) 31 to 35
CERTIFICATIONS
Compliance to Medical Device Rules (MDR) 2017 as amended till date Yes
Availability of valid Medical Device license for the product issued from the competent  
Valid Medical Device License Number MFG/MD/2021/000143
Certification for manufacturing unit ISO:13485 (Latest)
Availability of Test Report for each supplied batch/product as per Medical Device Rule (MDR) 2017 as amended till date Yes

SHELF LIFE
Shelf life from the date of manufacture (Years) 3 year


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RADHAKRUSHNA MEDICALS

Yavatmal, India

Business Operations: Merchant

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Product Description Hernia Fixation Device
Purpose For fixation of mesh during hernia procedure
PRODUCT INFORMATION
Fixation material Non Absorbable material
Type of fixation Single Point
Material of Tack/Glue Titanium
Mode of Firing for device Manual
Duration of Absorbtion NA in case of Non Absorbable
MRI Compatibility Yes
Number of Fasteners/Hooks 30
Length of Fasteners/Hooks (±0.5 mm) 3 mm to 5 mm
The fixation device shall have indicator regarding usage of fasteners/hooks and remaining tackers Yes
Length of the fixation canulla of device in Centimeter (±0.5 mm) 31 to 35
CERTIFICATIONS
Compliance to Medical Device Rules (MDR) 2017 as amended till date Yes
Availability of valid Medical Device license for the product issued from the competent authority defined under Drugs and Cosmetic Act 1940 and Rules made there under as amended till date Yes
Valid Medical Device License Number MFG/MD/2021/000143
Certification for manufacturing unit ISO:13485 (Latest)
Availability of Test Report for each supplied batch/product as per Medical Device Rule (MDR) 2017 as amended till date Yes
Submission of all necessary certifications, licenses and test reports to the buyer at the time of bid submission or along with supplies as per buyer requirement Yes
SHELF LIFE
Shelf life from the date of manufacture (Years) 3 year
Minimum shelf life of the product at the time of delivery to the consignee 3/4 th of Total Shelf Life


Established in: 2021
Bussiness Type: Sole Proprietorship
Bussiness Type: Merchant
MSME: Yes
Countries exporting to: United States, Philippines, Smaller Territories of the UK, United Kingdom, Bangladesh, Pakistan, Nepal, United Arab Emirates, Australia, Malaysia, Canada, Korea North, Korea South, Thailand, Mexico, Saudi Arabia, Bulgaria, Russia, Poland, Ethiopia, Zimbabwe, Taiwan, Albania, Azerbaijan, Brazil, Tanzania, Bhutan, France, Kuwait, Egypt, Vietnam, Belgium, Belarus, Congo, Czech Republic, Germany, Greece, Greenland, Indonesia, Iran, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Liberia, Lithuania, Macedonia, Afghanistan
Export Turnover (3 years): US$10,000 to US$50,000
Countries would like to export to: Austria, United States, United Kingdom, Turkey, Thailand, Switzerland, Sri Lanka, South Africa, Bangladesh, Albania, American Samoa, Anguilla, Malaysia, Canada, Korea North, Japan, Korea South, Uzbekistan, Azerbaijan, Bhutan, Belgium, Australia, Afghanistan, Mexico, France, Ethiopia, Germany, Netherlands Antilles, Tanzania, Turks And Caicos Islands, Italy, Bulgaria, Greece, Greenland, Indonesia, Iran, Iraq, Congo, Latvia, Lebanon, Liberia, Lithuania, Kenya, Central African Republic, United Arab Emirates, Philippines, Algeria, Andorra
No of employees: 1-10

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