Auto-Disable Syringes
Single-use injection devices manufactured around controlled component production, repeatable assembly and disciplined quality review.
Auto-Disable Syringes: built as a system, not a part.
Auto-disable syringes are designed for immunization and injection programs where reuse prevention is essential. Kyoto's platform is manufactured through a controlled process that connects molded components, precision assembly, packaging and quality review inside a dedicated medical-device production environment.
Single-use safety architecture
The device is designed around an auto-disable mechanism intended to prevent reuse after the prescribed injection cycle. The exact mechanism description will match the approved product design and IFU.
Controlled component manufacture
Critical molded parts are produced with close attention to component consistency and assembly fit.
Cleanroom-controlled production
Assembly takes place within Kyoto's controlled medical-device manufacturing environment.
In-house quality integration
Production and QA teams work within the same manufacturing system, keeping inspection and feedback close to the line.
Scalable supply
The production platform is designed to support repeatable manufacturing as partner demand grows.
Configurations currently manufactured.
As supplied by the Kyoto product team. Dimensions in inches with millimetre equivalents.
| Product | Capacity | Needle gauge | Needle length |
|---|---|---|---|
| Auto-Disable Syringe with Needle | 3 ml | 23G | 1" (25 mm) |
| Auto-Disable Syringe with Needle | 5 ml | 23G | 1" (25 mm) |
- Sterility state
- Stated in datasheet / IFU
- Sterilization method
- Stated in datasheet / IFU
- Primary packaging
- Stated in datasheet / IFU
- Shelf life
- Stated in datasheet / IFU
- Applicable standard(s)
- Stated in datasheet / IFU
- Registration by market
- Stated in datasheet / IFU
Product specifications are subject to the approved product design and may vary by market. Refer to the current datasheet and Instructions for Use.
Documentation for tender and qualification.
Datasheets and IFUs are issued per revision. Regulatory documents are provided on request by market.
- On request
Product datasheet
Current revision issued on request.
- On request
Instructions for Use
Approved IFU for the product and market.
- Gated
Regulatory / registration documents
Provided by product and destination market.
- On request
Packaging specification
Primary and secondary packaging and case configuration.
Frequently asked.
An auto-disable syringe includes a mechanism intended to prevent the device from being used more than once after the prescribed injection. The exact mechanism used in Kyoto's platform is described in the approved product design and Instructions for Use.
The platform is currently offered in 3 ml and 5 ml capacities, each supplied with a 23G × 1" needle. Contact our team for market-specific availability.
Private-label programs are discussed as part of a manufacturing partnership conversation. Start a partnership brief and select 'Private label' under manufacturing requirements.
Use the 'Request samples' action on this page or submit a product requirement through the contact page. Our team routes the request to the appropriate commercial contact.
Datasheets, Instructions for Use and packaging specifications are listed under product downloads. Regulatory and quality documents are provided on request according to product and market.
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Evaluating auto-disable syringe supply?
Share the required capacities, needle configurations, annual volume, destination markets and packaging requirements. Our team routes your request to the appropriate technical and commercial contacts.