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📦 If imported for use in the manufacture of sterile surgical sutures

If imported for use in the manufacture of sterile surgical sutures

HS Code:

📦

Overview

The category 'If imported for use in the manufacture of sterile surgical sutures' falls under the Harmonized System (HS) Code related to medical products and materials, likely under Chapter 30 (Pharmaceutical Products) or Chapter 90 (Optical, Photographic, Medical or Surgical Instruments). This category specifically includes raw materials or components imported explicitly for the production of sterile surgical sutures, which are critical medical devices used in surgeries to close wounds. These materials must meet stringent regulatory standards for sterility and biocompatibility. Global trade in this category is driven by the demand for high-quality medical supplies, advancements in surgical techniques, and the increasing number of surgical procedures worldwide.

Total Trade Volume

Approximately $1.2 billion USD

Data from 2022

Source

United Nations Comtrade Database & World Trade Organization (WTO) Statistics

Tariff Analysis

Average Rate

5.5% ad valorem

Highest Rate

12% (applied by certain developing countries to protect domestic industries)

Lowest Rate

0% (under free trade agreements or for Least Developed Countries under preferential schemes like GSP)

Common Restrictions

  • Stringent quality and sterility certification requirements (e.g., ISO 13485)
  • Import licensing for medical-grade materials
  • Compliance with Good Manufacturing Practices (GMP)
  • Restrictions on non-biocompatible materials

Market Trends

Rising demand for minimally invasive surgeries

Increased need for advanced suture materials, boosting imports of specialized raw materials for sterile sutures.

2021-2023

Growth in medical tourism in Asia-Pacific

Higher demand for surgical supplies in countries like India and Thailand, leading to increased imports for manufacturing.

2022

Shift towards bioabsorbable sutures

Growing imports of synthetic and natural polymers used in bioabsorbable suture production.

2020-2023

Recent Developments

EU Medical Device Regulation (MDR) Update

The European Union tightened regulations under the MDR framework, requiring stricter compliance for materials used in sterile surgical sutures.

May 2021

Increased costs for exporters to the EU due to additional certification and testing requirements, potentially shifting trade to less regulated markets.

US-China Trade Agreement Phase 1

Reduction in tariffs on certain medical raw materials, including those for sutures, as part of the Phase 1 trade deal between the US and China.

January 2020

Facilitated higher export volumes from China to the US, strengthening China's position in the market.

India's PLI Scheme for Medical Devices

India launched the Production Linked Incentive (PLI) scheme to boost domestic manufacturing of medical devices, including surgical sutures.

March 2021

Encouraged local production but also increased imports of high-quality raw materials to meet production standards.