Medical Document Library
Direct access to official 2026 medical device catalogues, clinical monographs, ISO 13485 & WHO-GMP certificates, CDSCO regulatory records, and Mecca Labs formulations.
Mecca Healthcare Comprehensive Medical Device Catalogue 2026
Complete reference catalogue encompassing 97+ sterile medical devices across Infusion (including Needle-Free closed systems), Anesthesia, Urology, Cardiology, Dialysis, Surgery, and Gastroenterology.
Mecca Healthcare Official Product List (CDSCO Verified)
Concise statutory SKU reference list with active CDSCO license brand names, item codes, pack sizes, and standard carton quantities.
CDSCO Complete Product Category Classification List
Statutory Central Licensing Authority documentation detailing medical device risk classifications (Class A/B/C) and clinical indications.
Nephrology Care & Dialysis Solutions Catalogue 2026
Dedicated clinical handbook detailing hemodialysis catheters, AV fistula needles, peritoneal catheters, and extracorporeal bloodline sets.
Hemodialysis Catheter Kit Technical Detailer
Engineering specifications and Seldinger guide for short-term and long-term hemodialysis access kits with primed lumen capacities.
LifeGuard Dial Flow Regulators Product Presentation
Comprehensive monograph covering precision micro-dial administration sets offering consistent flow delivery from 5 to 250 ml/hr.
Central Venous Catheter (CVC) Kit Clinical Monograph
Single, double, and triple lumen central venous catheter kits designed for continuous CVP monitoring, high-volume infusion, and blood sampling.
Needle-Free Connectors (NFC) & Closed Drug Delivery Range
Closed vascular access systems, swabable valves, and extension lines engineered to eliminate sharps injuries and prevent bloodstream infections.
ISO 13485:2016 Medical Devices Quality Management Certificate
Official QMS certificate accredited for design, extrusion, molding, cleanroom assembly, and sterile packaging of single-use medical devices.
ISO 9001:2015 Quality Management System Accreditation
Enterprise quality management certification assuring continuous process control and traceability across all manufacturing plants.
WHO–GMP Certificate of Good Manufacturing Practices
World Health Organization Good Manufacturing Practices validation issued by FDCA Gujarat for sterile medical disposable production.
European CE Mark Quality Assurance Notification
Official European Conformity Assessment certification authorizing export distribution of sterile medical devices under European directives.
CDSCO Form MD-9 State Manufacturing Licences
Statutory licensing issued by the Central Licensing Authority for medical device manufacturing facilities at Kalol and Boranada (Jodhpur).
Mecca Labs Pharmaceutical Formulations Catalogue
Complete portfolio of sterile pre-filled syringes, beta-lactam antibiotics, oral liquids, tablets, dry syrups, and IV infusions.
Mecca Labs Domestic Nutraceutical & Wellness Catalogue
FSSAI-registered dietary supplements, multivitamins, omega-3 softgels, calcium minerals, and effervescent daily wellness formulations.
Mecca Labs Global Export Grade Nutraceutical Catalogue
Export-grade botanical extracts, advanced herbal formulations, dietary capsules, and health syrups engineered for worldwide distribution.
Mecca Labs Infant Milk Formula & Pediatric Nutrition Catalogue
Scientific infant nutrition formula stages 1 to 3, maternal wellness formulas, follow-on milk powders, and pediatric dietary cereals.
Mecca Labs Cosmeceutical & Aesthetic Dermatology Catalogue
Dermatologist-tested skincare, human intimate hygiene products, and La Splendra aesthetic beauty solutions backed by ISO 22716 GMP.
OEM Contract Manufacturing & Loan-License Blueprint
Detailed blueprint explaining turnkey medical device contract manufacturing, private labeling, custom mold tooling, and Cleanroom Class 10,000 capabilities.
Mecca Healthcare Corporate Governance & Manufacturing Tour
Corporate documentary summarizing 48+ years legacy, founder ideals, active manufacturing facilities in Gujarat and Rajasthan, and worldwide export presence.
Require Custom Drug Master Files (DMF) or Batch CoA?
Our in-house Regulatory Affairs team supplies validated Certificate of Analysis (CoA), bioburden assay test results, CE technical files, and localized MOH dossier documentation for international tenders and institutional procurement.