- Overview
- GTK Strong Quality System
- GTK Core Strength
- Detailed Photos
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- Packaging & Shipping
- GTK Certifications
- FAQ
Basic Info.
Model NO.
HSD-40/C
Material
Plastic
Feature
Disposable
Certification
CE, FDA, ISO13485
Group
Adult
Diameter
5mm
Customized
Yes
Transport Package
Blister Package
Specification
40ml volume
Trademark
TK
Origin
China
HS Code
901890
Production Capacity
300000 Pieces/Year
Product Description
Suitable for laparoscopic procedures disposable medical Endo bag/Endobag/retrieval bags.
G T.K Medical is one of the top China manufacturers with 17 years manufacturing experience.
G T.K Medical is one of the top China manufacturers with 17 years manufacturing experience.
GTK Medical, established on March 3, 2004, is a hi-tech medical device manufacturer which focuses on the R&D and manufacturing surgical devices like trocars, retrieval bags for more than 20 years. 
GTK Medical passed GMP of NMPA(CHINA FDA) AND US FDA factory registration (No. 3008191256) and ISO13485:2016 medical devices quality management system.
| Q: Are you a factory or trading company? |
| A: Yes. We are a factory in China with 20 years surgical devices developing and manufacturing experience. |
| Q: What is the core strength of GTK Medical? |
| A: Our core strength is strong R&D Capability (more than 600 patents applied) and world first class quality (FDA 510K, CE, ISO13485:2016) management on products. |
| Q: What makes GTK Retrieval Bags stand out? |
| A: Excellent retrieving performance plus excellent soft medical bag to ensure safety and efficacy. |
| Q: Do you provide free samples of GTK Retrieval Bags for clinical trial use? |
| A: Yes. We are proud and confident to provide free samples for real clinical testing and evaluation. |
| Q: Do you have exported experiences to large medical devices company/companies? |
| A: Yes. We exported to more than 40 countries, most of which are based in the America and Europe. |
| Q: Do you accept factory audit prior to formal partnership? |
| A: Yes. We are proud and confident to accept factory audit. We passed US FDA on site aduits on 2015 and 2021. |
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