Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery

Product Details
Customization: Available
Type: Retrieval System
Application: Abdominal, Microsurgery
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Manufacturer/Factory & Trading Company

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Audited by an independent third-party inspection agency

Number of Employees
138
Year of Establishment
2004-03-03
  • Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery
  • Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery
  • Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery
  • Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery
  • Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery
  • Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery
Find Similar Products
  • Overview
  • GTK Strong Quality System
  • GTK Core Strength
  • GTK Retrieval Bags details
  • GTK Products Sepcifications
  • GTK Certifications
  • FAQ
Overview

Basic Info.

Material
Plastic
Feature
Disposable
Certification
CE, FDA, ISO13485
Group
Adult
Diameter
10mm
Customized
Yes
Bag Size
80mm
Volume
200ml
Remark
for Adult Surgery
Transport Package
Blister Package
Specification
80ml volume
Trademark
TK
Origin
China
HS Code
901890
Production Capacity
300000 Pieces/Year

Product Description

Endoscopic instruments Retrieval bags for laparoscopic surgical incision for Cholecystectomy top China manufacturer 
 
GTK Strong Quality System

GTK Medical is a hi-tech medical devices manufacturer of more than 20 years R&D and manufacturing expertise. GTK veress needles are exported to more than 40 countries and used in more than 1000 hospitals worldwide. 

Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery

Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery
Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery

 

GTK Core Strength

GTK Medical passed GMP of NMPA(CHINA FDA) AND US FDA factory registration (No. 3008191256) and ISO13485:2016 medical devices quality management system. 

Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery

GTK Retrieval Bags details


Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery

 

Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery

Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery
GTK Products Sepcifications

Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery

 

GTK Certifications
Founded in 2004, G T.K Medical has applied more than 700 Patents at home and abroad, including more than 30 PCT Patents.
 

Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery

FAQ
Mdr CE Certificate Laparoscopic with Retrieval Bags Endobag Specimen Retrieval for Surgery
 
Retrieval Bags
Q: Are you a factory or trading company?
A: Yes. We are a factory in China with 20ears 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 700 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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