Regulatory support services for medical device market registration, including technical documentation preparation and compliance verification. Facilitates product launch and government approval processes.
Manufactured by
Zhongguancun International Medical Inspection and Certification Co. Ltd.
China
Zhongguancun International Medical Inspection and Certification Co., Ltd. (ZIC) is a national high-tech enterprise specializing in testing and inspection of disinfection products, food, cosmetics, and water-related products. The company holds CMA certification for 4,000+ testing capabilities and CNAS certification for 600+ capabilities, with 21 functional laboratories across 10,000+ m² facilities including Class 100 cleanrooms and SPF-grade animal facilities.
✦ Product-Specific Coverage
Based on AI-matched alternatives related to this product across Suplivia's medical sourcing network.
Generated for this product
AI-matched supplier coverage based on related product alternatives.
JiangSu Ailu Optoelectronics Technology Co., Ltd.
China · 1 relevant product
Point Share Medicine Technology (Shanghai) Co., Ltd.
China · 1 relevant product
SAXOCON A/S
Denmark · 1 relevant product
77 more relevant manufacturers available
Get free access to all relevant manufacturers for this product.
See all manufacturers →21 more sourcing countries available
Get free access to all sourcing countries identified for this product.
See all countries →See the full supplier coverage for this product
Get free access to all relevant manufacturers, sourcing countries, and product alternatives.
✓ Free for medical industry professionals.
from other manufacturers
from other manufacturers
3 of 111 closest product alternatives
JiangSu Ailu Optoelectronics Technology Co., Ltd. · China
Specialized service supporting regulatory registration and compliance documentation for endoscope systems and components. Assists manufacturers in meeting medical device regulatory requirements for market approval.
Point Share Medicine Technology (Shanghai) Co., Ltd. · China
Regulatory registration and testing service for active medical devices, passive medical devices, and in vitro diagnostic reagents. Supports compliance with medical device classification, clinical evaluation, and submission requirements for market authorization in regulated territories.
SAXOCON A/S · Denmark
Expert regulatory support for medical device approval including MDR and FDA compliance guidance. Provides data-driven safety dossiers and toxicological risk assessments to accelerate time-to-market globally.
108 more product alternatives available
Create a free account to compare more product alternatives and supplier options.
© 2026 Suplivia · Home · Browse Products