Contact Us
Ready to start your medical device project? Fill out the form below and our team will respond within 24 hours.
Direct Contact
For urgent inquiries, please email us directly at [email protected]
Our Commitment
- ✓ Response within 24 business hours
- ✓ Confidential project discussion
- ✓ Detailed project quote with timeline
- ✓ ISO 13485:2016 certified manufacturing
Key Takeaways
- ✓ Contact Dinghmed for OEM/ODM medical device manufacturing inquiries: quotes, technical questions, and partnership discussions.
- ✓ Our team responds to most inquiries within 24 business hours, with dedicated regulatory and engineering contacts for active projects.
- ✓ For fastest response, include your product category (first aid kits, hemostatic agents, trauma care), target market, and estimated annual volume.
- ✓ All communications are confidential under mutual NDA when requested, with IP protection aligned to ISO 13485 and FDA requirements.
Frequently Asked Questions
How quickly will Dinghmed respond to my inquiry?
We respond to most inquiries within 24 business hours. For urgent regulatory or production questions related to active projects, dedicated contacts are available for same-day response.
What information should I include in my project inquiry?
For fastest and most accurate response, include: product category (first aid kit, hemostatic gauze, trauma care), target market (US FDA, EU MDR, or other), estimated annual volume, and any specific certifications required. This allows us to route your inquiry to the right specialist.
Can I sign an NDA before sharing product details?
Yes. We routinely sign mutual NDAs before detailed technical discussions. Our standard NDA template is aligned with medical device industry practices and protects both parties' intellectual property.
Do you have dedicated regulatory affairs contacts?
Yes. Our regulatory affairs team handles FDA submissions, EU MDR technical documentation, and CE marking. For active projects, you will be assigned a dedicated regulatory contact alongside your project manager.
Where is Dinghmed located and can I visit the facility?
Our manufacturing facility is ISO 13485:2016 certified and FDA registered. Site visits can be arranged for qualified partners — contact us to schedule a facility tour and audit.