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Events & exhibitions

Event recap · Shanghai

BIO at Medtec China 2026

Medtec China 2026 ended on September 3. In Shanghai, BIO met medical-device teams to discuss implant-grade silicone, processing and documentation for catheter and drug-delivery applications.

Visitors seated at the Avantor NuSil exhibit beneath a medical-silicone application display during Medtec China 2026
Medtec China 2026 onsite · September 1, 2026 · Avantor NuSil, booth 2C302 · Photo provided by BIO

Event facts

Date
September 1–3, 2026
Venue
SNIEC · Halls N1–N4
Edition
20th Medtec China
BIO focus
Medical-silicone technical exchange

Exhibition recap

Silicone applications discussed in Shanghai

During the show, BIO held face-to-face technical discussions with medical-device professionals around implant-grade silicone, catheter and hormonal drug-delivery applications, material processing and documentation needs. The discussions covered how to narrow the list of grades, what to check before evaluation and which current documents should accompany a sample.

Before screening grades, identify the device component and intended process, the documents the team needs and the tests planned for the finished device.

Three days of discussions on silicone selection, processing and documentation.

Implant-grade silicone at the Avantor NuSil exhibit

At the Avantor NuSil exhibit, booth 2C302, the displays photographed on September 1 illustrated roles for implant-grade silicone in catheters and hormonal drug-delivery devices. The official exhibitor directory also listed liquid silicone rubbers, lubricious silicones and silicone adhesives among the exhibit's product categories.

For each device, check contact type and duration, geometry, mechanical requirements, processing, sterilization and current documentation. Include finished-device validation in the selection plan.

The exhibit examples described here are observations from the show, not a finished-device suitability, regulatory or performance conclusion. Product identity, current documentation and validation requirements must be confirmed for each project.
Visitors seated beneath an implant-grade silicone catheter application display at the Avantor NuSil exhibit
Visitors seated beneath a catheter-application display · September 1, 2026 · Photo provided by BIO

Three takeaways

Questions for material selection

01

Define the device requirements

Define the component, contact conditions, process and required evidence before selecting a product code.

02

Check data and processing requirements

Compare candidate materials against your processing conditions and performance targets using current documents.

03

Record open questions

Record the open questions, who will answer them and what evidence is still needed.

Application support

Discuss your device project

Tell BIO what you are developing, the contact conditions, intended process, target material properties and document needs.

Sources and photo note