Registered Office & Cleanroom Facility
Universal Sutures (Unisur Lifecare Pvt. Ltd.) operates an advanced ISO 13485 certified cleanroom manufacturing facility in Bengaluru, India. We serve hospital networks, medical device distributors, and private-label brand owners across more than 80 countries worldwide.
Corporate & Manufacturing Address
No.15/1,2,3, 1st Floor, Acharya Industrial Complex, Andrahalli Main Road, Vishwaneedam Post, Bengaluru Urban, Karnataka 560091, IndiaOperating Hours & Timezone
Monday to Saturday: 9:00 AM – 6:45 PM IST (UTC +5:30) Off Days: 1st & 3rd Saturday of every month, and SundayRegulatory Credentials & Quality Systems
Certifications: EU MDR (Regulation 2017/745), CE Marking, EN ISO 13485:2016 Quality Assurance: Batch-released with Certificate of Analysis (CoA) & validated EO sterilisation cyclesSpecialized Business Departments
Get connected directly with our dedicated business units to ensure rapid, professional technical and commercial assistance for your market.
International Business (Overseas Sales)
Global distributor partnerships, regional agency tenders, and direct container shipments. Phone: +91-910-899-0400 / +91-910-899-0407 Email: [email protected]OEM & Private Label Division
Custom suture materials, needle configurations, artwork design, and multi-language retail packaging. Phone: +91-910-899-0400 Email: [email protected]Domestic Tenders & Hospital Supply
Institutional hospital tenders, government healthcare contracts, and domestic distributor support. Phone: +91-910-899-0414 / +91-910-899-0416 Email: [email protected]Quality Affairs & Regulatory Dossiers
Technical files, CE dossier support, stability data, and country-specific registration dossiers. Phone: +91-910-899-0401 Email: [email protected]Human Resources & Global Talent
For career inquiries, technical cleanroom engineering positions, or quality management opportunities, contact HR Team at +91-910-899-0422.
Why Global Healthcare Buyers Partner With Universal Sutures
EU MDR 2017/745 Certification
Universal Sutures is among the elite medical device manufacturers in India to achieve comprehensive EU MDR certification across 13 distinct product families, ensuring compliance with strict European medical safety regulations.
1.1× USP Strength Requirement
Every absorbable and non-absorbable suture batch is tested to exceed pharmacopoeial minimum tensile strength and needle attachment pull standards by at least 10%, offering superior security during surgical closure.
End-to-End Turnkey OEM Solutions
From initial thread extrusion, precision needling, multi-layer foil pouch sealing, to validated Ethylene Oxide (EO) terminal sterilisation, we provide complete private-label manufacturing and process transfer.
Request Technical Dossiers or Product Catalog
Connect with our global technical team to request product samples, complete technical specification sheets, CE certificates, or full product catalogs for your market registration.