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Supplied by YOKO
YOKO-YGF-K
YOKO-YGF-K is an automatic filling and stoppering family for prepared prefilled syringes. The reference range includes one-, two-, and five-head configurations, common syringe volumes from 0.5 to 20 mL depending on model, and listed capacities from 600 to 3,600 syringes per hour. Selection requires the actual syringe and stopper, product characteristics, filling path, environmental strategy, vacuum stoppering requirement, accuracy method, and downstream handling plan.
Equipment purpose
The system is intended to fill compatible liquids or validated viscous products into ready-to-fill syringe barrels and insert the stopper with controlled handling. It supports projects that need a repeatable bridge between component preparation and downstream inspection, plunger-rod assembly, labelling, or secondary packaging.
Operating sequence
Syringe barrels are fed or presented in the required orientation and indexed to one or more filling heads. A configured metering system delivers the dose, after which the stopper is positioned and inserted, with vacuum assistance where specified to reduce trapped air and stopper friction. Performance depends on barrel and stopper tolerances, silicone condition, product rheology, dose, pump selection, filling speed, environmental control, and component presentation.
Process fit
Use these references to frame the first technical discussion. Suitability is confirmed with actual material, format, and process data.
Reference parameters
Values are model references for initial selection. The quotation and approved technical agreement define the final supplied configuration.
| Model | YOKO-1YGF-K / YOKO-2YGF-K / YOKO-5GF-K |
|---|---|
| Applicable Materials | liquid and ointment / liquid and ointment / liquid and ointment |
| Applicable Syringe Specifications (mL) | 0.5, 1, 2.25, 3, 5, 10, 20 / 0.5, 1, 2.25, 3, 5, 10, 20 / 1 (Long),1, 2.25, 3 (standard), 5, 10 |
| Number of Filling Heads | 1 / 2 / 5 |
| Number of Plugging Heads | 1 / 2 / 5 |
| Filling Accuracy | ≤±1% / ≤±1% / ≤±1.5-2% |
| Capacity (pcs/hr) | 600-900 / 1200-1800 / 2400-3600 |
| Power Supply | Configured for the destination electrical standard |
| Compressed Air | 0.55-0.75 MPa 15 L/S / 0.55-0.75 MPa 15 L/S / 0.55-0.75 MPa 40 L/S |
| Dimensions (mm) | 800 × 700 × 1730 / 1088 × 858 × 1800 / 1880 × 3950 × 1860 |
| Weight (kg) | 300 / 500 / 1900 |
Before quotation
A useful quotation starts with the product, container or format, target output, available utilities, and destination requirements.
Ask for the current datasheet, layout information, and available documentation package.
Request documentsSupporting files
Availability varies by model and configuration. Request the current demonstration, datasheet, layout, or documentation package when needed.
Ask whether a current model demonstration is available.
Model-specific operating manuals and layout files are supplied after configuration review.
Selection questions
The catalogue lists common formats from 0.5 to 20 mL, but coverage differs by model. Send drawings and samples for the barrel, flange, tip, stopper, and nest or tray where applicable. Long-barrel and standard formats can require different handling, so the approved format list must be part of the technical agreement.
Agree the nominal dose, allowable variation, sampling plan, measurement method, product temperature, priming method, run speed, and treatment of startup units. Gravimetric or volumetric methods may give different uncertainty depending on density and dose. Accuracy should be verified with the intended pump, nozzle, product, and syringe.
Vacuum can help control the air space and reduce the force needed to position a stopper without a plunger rod pushing it through the barrel. The required vacuum level, insertion depth, stopper lubrication, barrel silicone, product headspace, and acceptable bubble condition should be established with actual components.
Not unless the quotation explicitly includes it. The machine, restricted-access or isolator system, component preparation, transfer, filtration, cleaning, sterilization, environmental monitoring, interventions, and qualification responsibilities must be defined as one process. Regulatory suitability cannot be inferred from stainless-steel construction or a filling-machine model alone.
Provide enough production-intent syringes and stoppers for setup and the agreed run, plus product or a representative material with documented viscosity and density. Include drawings, storage conditions, target dose, stopper position, bubble acceptance, speed, sampling, reject criteria, cleaning expectations, and any downstream interface that affects discharge.
Model-level review
Share the material, product format, target sustained output, available utilities, destination standard, and expected documentation scope.
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