Define the barrier
State moisture, oxygen, light, microbial and tamper-evidence requirements without assuming one material solves every risk.
Configure a flat-plate blister line around the actual syringe, blister drawing, forming depth, loading method and lidding material. HIJ starts from the documented DPP-260/360K platform and freezes syringe-specific tooling through sample trials.
It is a blister forming, loading, sealing, coding and cutting system configured to protect a syringe in a dimensioned cavity. The syringe is not a free-flowing tablet: its barrel, plunger, flange, tip cap and needle shield make cavity depth, orientation and gentle loading central to the project.
The machine cannot define the package alone. The barrier target, syringe condition, sterilization route, opening method and shelf-life study determine the forming web, lidding and seal-validation work.
| Material path | Verified platform position | Project decision |
|---|---|---|
| PVC / PVC-PVDC / PE forming web | Listed in the DPP-260/360K material specification; positive-pressure forming is documented. | Confirm thickness, roll geometry, cavity depth, syringe retention and the selected lidding seal window. |
| Alu/PVC with aluminum lidding | Documented flat-plate Alu/PVC packaging configuration with coated PTP aluminum foil. | Confirm peel or push-through opening behaviour, printing and seal-integrity protocol. |
| Cold-form Alu/Alu | Alu/Alu function is documented. Standard forming depth is 12 mm; the source lists 25 mm for a special machine. | Compare the complete syringe envelope with the special tooling limit before quotation. |
| PET-G or Tyvek combinations | Not proven as standard materials in the current DPP-260/360K file. | Require film supplier data, forming/sealing trials and written confirmation of station changes before purchase. |
State moisture, oxygen, light, microbial and tamper-evidence requirements without assuming one material solves every risk.
Clarify whether the syringe arrives sterile, the package is sterilized after sealing, or the blister is only secondary protection.
Set seal strength, leak or integrity testing, opening behaviour and stability evidence in the customer quality plan.
The documented machine sequence covers web handling through punching. Syringe loading is inserted as a project-specific station between forming and inspection.
Motor-assisted roll unwinding reduces traction resistance and monitors the end of the forming web.
Contact heating softens the web before positive compressed-air forming creates the specified cavity.
Use the approved manual, fixture-assisted or custom manipulator method without disturbing the plunger, cap or shield.
Confirm presence and position before sealing. Camera detection and reject logic must match the approved inspection scope.
Flat-plate heat sealing joins the lidding to the formed web; pressure, temperature and dwell belong in the recipe and OQ.
Batch information is impressed and mechanical or servo traction advances the web at the selected stroke.
The punch cuts the agreed blister layout; an optional plate-suction device can support downstream conveyor transfer.


These values come from the formal DPP-260/360K file. They describe the blister platform, not a guaranteed syringe output. HIJ must calculate the finished result from the syringe and blister layout.
| Parameter | Published reference | Syringe-project note |
|---|---|---|
| Platform | DPP-260/360K flat-plate medium-speed Alu/PVC and Alu/Alu blister machine | Medical-device and ampoule applications are included in the documented scope. |
| Maximum forming area | 245 × 112 mm | Fit the full blister layout, flange clearance and cutting margin inside this envelope. |
| Maximum forming depth | 12 mm standard; 25 mm special machine | Compare against the largest syringe diameter, cap or shield and retention geometry. |
| Feed stroke | 40–120 mm adjustable | The selected blister pitch must remain within the usable stroke. |
| Maximum blanking reference | 40 cycles/min for standard 57 × 80 mm × 4 Alu/PVC layout | This is a cycle reference, not a guaranteed syringe blister output. |
| Forming web | Pharmaceutical PVC, typically 0.25–0.30 mm; published range 0.15–0.50 mm | Final material and thickness require forming trials. |
| Lidding | Single-side coated PTP aluminum foil, 0.02–0.025 mm | Other lidding such as Tyvek requires separate written technical confirmation. |
| Total power | 11 kW, three-phase 380 V 50 Hz; 220 V 60 Hz listed | Confirm site electrical standard and the load of project options. |
| Compressed-air flow | 0.25 m³/min reference | Confirm clean, dry air pressure and quality in the utility schedule. |
| Machine dimensions | 4470 × 1100 × 1740 mm | Allow clearance for rolls, tooling, loading and maintenance. |
| Machine weight | 3000 kg | Reference machine weight for floor-loading and handling review. |
| Traction | Mechanical or servo traction | Servo traction supports accurate, adjustable web advance when specified. |
| Controls reference | Siemens HMI/PLC/servo/inverter; Omron detection components | The formal list states that final configuration is subject to the contract. |
Loading usually becomes the limiting station because the syringe must arrive in the correct orientation without moving the plunger or damaging the cap, shield, flange or printed barrel.
The base source includes missing-product detection and reject capability. Syringe-specific camera checks should be selected from the actual defect list, not added as a generic “vision system”.
These inputs control the machine format, loading method, material trials, inspection, documentation and project price.
Dimensioned drawings, samples, barrel material, flange, plunger, tip cap, needle shield and acceptable contact points.
Units per pack, orientation, cavity depth, opening method, retention requirement and cutting outline.
Forming web, lidding, thickness, roll dimensions, artwork, sealing window and supplier samples.
Sustained accepted packs per minute, batch size, shifts, loading availability and changeover frequency.
Inspection defects, integrity tests, sterilization route, traceability, qualification documents and release criteria.
Upstream handling, downstream cartoning, coding, rejection, utilities, room layout and data requirements.
Agree the sample quantity, run duration, acceptance rate, reject definition and open-item process before FAT. Documentation such as DQ/IQ/OQ protocols is supplied only when included in the approved contract scope.
The approved URS, tooling drawing, samples and FAT results own the final machine configuration.
Send the six inputs below. HIJ can return the platform, tooling, loading, inspection, documentation and FAT scope as separate quotation items.