
Disposable Endo Retrieval Bag Model B (Titanium sheet)

Disposable Endo Retrieval Bag Model A (Titanium wire)


specimens to be placed. The bag body is made of high strength TPU material with good biocompatibility, soft and high strength.
The bag body can be retractable, convenient for intraoperative use.
The bag body has a variety of specifications to meet different surgical needs.
Can be through the 10mm puncture device, convenient operation.




Product Name | Disposable Endo Retrieval bag |
Appreance | Should be flat, smooth, no edge, no burr and crack and other defects |
Performance | The connections between the double-ring handle and the outer casing, and the single-ring handle and the inner casing in the retrieving bag should be firm and can withstand the pulling force of 10N without disconnecting or breaking; The carrier bag type A should be able to withstand the pull force of 10N, without the phenomenon of breaking away from the support ring; The sleeve, handle and opening device of the bag are moderately tight, which is convenient for operation; After the release of the carrier bag of the carrier bag, the opening can be fully opened, and the thermal bonding stripping force of the carrier bag is more than 8N; The rope of WPDB type bag and the bag should be able to withstand the pulling force of 10N for 5s, and the bag and the string should not be separated |
The test liquid should be colorless and transparent; The pH difference between the test liquid and the blank control liquid of the same batch should not exceed 2.0; The color of the test solution shall not exceed that of the standard control solution with mass concentration ρ (Pb2+) =1μg/ mL | |
Sterility | Sterilized with ethylene oxide |
Residual EO | After sterilization with ethylene oxide, the residual ethylene oxide should not be more than 10μg/g |

1. Professional global regulatory consulting team
The company leader Dr.Louis Li, has more than 10 years of experience in medical device quality management and product registration at home and abroad who previously served as Quality Engineering Supervisor at Zimmer Biomet, Management Representative and QA Manager at Medtronic Comfort, later Quality Regulation Director at Scion US and Scion China. Completed many F*D*A 510K applications and CE product registration in EU, and organized several F*D*A audits in the United States and large-scale international audits by ANVISA in Brazil.
2. Very good relationship with manufacturers in China
We assisted the Chinese factories to get CE/ISO/F*D*A certificate, we support factories to maintain their certificate every year, so we have good cooperation with different factories. We also invested several factories as a small shareholder, so we can get the direct factory wholesale price.
3. Professional research & development, quality control and sales team
We have good contact with advanced global medical company's experts. Also attend their summit to keep knowledge of latest medical industry technology or products. Most of our employees are highly educated.

Q: What is your strength in this field?
Q: Do you provide samples? Is it free or extra?
Q: Does your product have a warranty period?










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