Frequently Asked Questions
Frequently Asked Questions
Q: Does Creganna-Tactx Medical sell finished medical device or needle products?
A: No, Creganna-Tactx Medical is a contract designer and manufacturer and we do not manufacture or distribute finished medical devices for sale to market. We work solely on behalf of our customers - medical device and lifescience companies.
Q: I thought Creganna-Tactx Medical just offered manufacturing technologies for hypotubes?
A: Hypotubes are just one aspect of an extensive product & service portfolio offered by Creganna-Tactx Medical. This portfolio of technologies includes, but is not limited to, hypotubes, complex micro molded assemblies, insert molding, medical balloons, extrusions & braided tubing, advanced material, specialty needle design & manufacturing, contract design and prototypes.
Q. Will Creganna-Tactx Medical manfuacture a stent on behalf of my company?
A: No, Creganna-Tactx Medical does not offer stent processing technologies. Our focus is on technologies to design and build delivery devices. For finsihed device builds we can coordinate to provide stent assembly services for the delivery device.
Q. Do Creganna-Tactx Medical make guidewires?
A: While Creganna do not offer manufacturing services for standard workhorse guidewires we are in a position to work with clients on wire-based technologies integrated into advanced delivery systems. For example, we offer a wire-based component added to a metal tube as a transisiton feature for catheter distal assemblies and we provide wire braiding for advanced delivery devices.
Q: Can I come to visit Creganna-Tactx Medical?
A: Yes, Creganna operate an Open Door Policy for customers at all sites. Contact your Customer Account Manager or Sales Representative to arrange a visit.
A: No, Creganna-Tactx Medical does not offer stent processing technologies. Our focus is on technologies to design and build delivery devices. For finsihed device builds we can coordinate to provide stent assembly services for the delivery device.
Q. Do Creganna-Tactx Medical make guidewires?
A: While Creganna do not offer manufacturing services for standard workhorse guidewires we are in a position to work with clients on wire-based technologies integrated into advanced delivery systems. For example, we offer a wire-based component added to a metal tube as a transisiton feature for catheter distal assemblies and we provide wire braiding for advanced delivery devices.
Q: Can I come to visit Creganna-Tactx Medical?
A: Yes, Creganna operate an Open Door Policy for customers at all sites. Contact your Customer Account Manager or Sales Representative to arrange a visit.
Q. Is everything manufactured by Creganna-Tactx Medical in Ireland?
A: No, Creganna-Tactx Medical has manufactruing facilities in California, Minnesota, Massachusetts, Ireland and Singapore. The location of manufacture of your product will depend on your individual technology requirements.
Q: How do I start a project with Creganna-Tactx Medical?
A: To start a project with Creganna-Tactx Medical, simply contact our sales team to discuss your project. If it’s within our capabilities an Account Manager and a project team will be assigned to work on your project from start to finish.
Q: What quality standards do Creganna-Tactx Medical adhere to?
A: The quality standards we adhere to are ISO13485:2003 and FDA 21 CFR Part 820.
Q: Is Creganna-Tactx Medical an FDA regulated contract manufacturer?
A: Yes Creganna-Tactx Medical is a registered FDA contract manufacturer. The FDA Establishment Registration Numbers are 3004193842 (Ireland & MA), 3004036480 (Campbell, CA Tactx Medical), 2183982 (Plymouth, MN Tactx Medical), 3006984791 (Singapore, Avalon Medical Services).
Q: What confidentiality can I expect and how will you protect my IP if I work with Creganna-Tactx Medical?
A: Customer confidentiality is extremely important in Creganna-Tactx Medical. Non Disclosure Agreements provide total confidence and under no circumstances will any customer information be shared.
Q: Who are your customers?
A: Creganna-Tactx Medical is a partner to the largest blue-chip global medical device companies and emerging medical technology worldwide. Confidentiality agreements preclude the public communication of Creganna-Tactx Medical customer names unless specifically agreed with the customer.
Q: What experience does your staff have?
A: Creganna-Tactx Medical staff have expertise in project management, product building, design, quality, materials, bio medical engineering, mechanical, industrial & LEAN solutions. Our staff have extensive experience in the medical device industry.
Q: Can I get product samples?
A: Yes, Creganna-Tactx Medical has standard marketing samples available on request that are non customer specific.
Q: How do I get my prototype efficiently scaled up to production volumes?
A: After successful completion of your prototype, the part will enter our Product Introduction Process (PIP) process. A dedicated project team, incorporating expertise in quality, validation, engineering, commercial and production is assigned to manage the part through to production. Continuous communication is given to the customer throughout the process.
A: The quality standards we adhere to are ISO13485:2003 and FDA 21 CFR Part 820.
Q: Is Creganna-Tactx Medical an FDA regulated contract manufacturer?
A: Yes Creganna-Tactx Medical is a registered FDA contract manufacturer. The FDA Establishment Registration Numbers are 3004193842 (Ireland & MA), 3004036480 (Campbell, CA Tactx Medical), 2183982 (Plymouth, MN Tactx Medical), 3006984791 (Singapore, Avalon Medical Services).
Q: What confidentiality can I expect and how will you protect my IP if I work with Creganna-Tactx Medical?
A: Customer confidentiality is extremely important in Creganna-Tactx Medical. Non Disclosure Agreements provide total confidence and under no circumstances will any customer information be shared.
Q: Who are your customers?
A: Creganna-Tactx Medical is a partner to the largest blue-chip global medical device companies and emerging medical technology worldwide. Confidentiality agreements preclude the public communication of Creganna-Tactx Medical customer names unless specifically agreed with the customer.
Q: What experience does your staff have?
A: Creganna-Tactx Medical staff have expertise in project management, product building, design, quality, materials, bio medical engineering, mechanical, industrial & LEAN solutions. Our staff have extensive experience in the medical device industry.
Q: Can I get product samples?
A: Yes, Creganna-Tactx Medical has standard marketing samples available on request that are non customer specific.
Q: How do I get my prototype efficiently scaled up to production volumes?
A: After successful completion of your prototype, the part will enter our Product Introduction Process (PIP) process. A dedicated project team, incorporating expertise in quality, validation, engineering, commercial and production is assigned to manage the part through to production. Continuous communication is given to the customer throughout the process.
| Ireland Tel: +353 91 757 801 |
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Marlborough, MA Tel: + 508 658 7100 |
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Plymouth, MN Tel:+1 763 559 6002 |
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Campbell, CA Tel:+1 408 364 7100 |
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Singapore Tel: +65 6468 1456 |
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