★ Sector

Medical &
Pharma.

FDA-grade medical device components and pharma equipment parts.

★ FDA / ISO 13485
35+
ISO 13485
18+
FDA Reg
USP VI
Class
★ Sector Overview

India is the world’s
“pharmacy”.

India supplies 20% of global generic drugs and is rapidly growing in medical devices. Magnus partners with 35+ ISO 13485 certified Indian suppliers for medical-grade machining, plastic injection, rubber/silicone, and assembly.

Strong concentrations in Bangalore, Hyderabad, Vadodara, Chennai — supplying global brands like Becton Dickinson, Stryker, Medtronic suppliers, B. Braun.

At a Glance

Medical suppliers35+ ISO 13485
FDA registered18+ facilities
USP Class VIYes (plastics/rubber)
CleanroomClass 8 / Class 7
Annual volume$10M+
★ Components We Ship

Sector
components.

CategoryComponents
Surgical InstrumentsForceps, retractors, scissors, scalpels, clamps, dilators, orthopaedic instrument bodies (SS 304L/316L)
Orthopaedic & ImplantsImplant blanks (Ti, CoCrMo), orthopaedic plates, screws, hip/knee components (non-final-form)
Lab & DiagnosticCentrifuge components, microscope parts, lab equipment housings, diagnostic device enclosures, slide trays
Disposable DevicesUSP Class VI plastic for syringes, IV sets, drainage systems, inhaler parts
Medical SiliconeSilicone tubing, gaskets, septa, valve diaphragms — USP Class VI and FDA-compliant
Pharma EquipmentSanitary valve bodies, tablet press parts, packaging machine components, stainless tanks
★ Sub-Segments

Where we ship
sector parts.

Surgical Tools

Reusable surgical instrument components.

  • Forceps bodies
  • Retractor parts
  • Endoscopy handpieces
  • Surgical scissors

Diagnostic Devices

In-vitro diagnostics.

  • IVD device housings
  • POC test cassettes
  • Glucose meter parts
  • Pulse oximeter parts

Pharma Equipment

Tablet, capsule, packaging machinery.

  • Tablet press dies
  • Capsule filling parts
  • Mixer/blender parts
  • Packaging machine parts
★ Why India

Cost. Quality.
Scale.

01

ISO 13485

Standard QMS for medical device manufacturing. All Magnus medical suppliers certified.

02

FDA 21 CFR 820

US FDA QSR compliance for design controls, CAPA, traceability. FDA establishment registration.

03

EU MDR 2017/745

Notified body audits, Technical Documentation, CE-MD marking. Class I, II, III support.

04

USP / Cleanroom

USP Class VI material certification, ISO 14644 Class 7/8 cleanroom assembly.

★ Frequently Asked

Sector
FAQs.

ISO 13485 + FDA support?
Yes. 35+ ISO 13485 suppliers, 18+ FDA-registered facilities. Magnus coordinates FDA establishment registration and 510(k) prep.
Cleanroom assembly?
Three suppliers offer ISO 14644 Class 7 or Class 8 cleanroom assembly. Common for sterile disposables, IVD components, implant packaging.
USP Class VI plastics?
Standard offering. PC (Makrolon Rx), PEEK, PSU, PPSU, COC, certain PP grades. Full biocompatibility test certificates included.
★ Sector Need?

Vetted suppliers
in 48 hours.