Low Pressure Polyurethane Machine
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Low-Pressure PU Foaming Machine | Medical Sponges

Configured dispensing for sponge formulations intended for medical applications; finished-product and process validation are separate requirements.

Pouring Rate

50~1000 g/s

Mix Ratio (Medical Polyol:MDI)

100 : 85~95

Metering Accuracy

≤ ±0.3% full range

Foaming Pressure

0.5~2.0 MPa

Availability on Request Delivery Schedule on Quotation 1‑Year Warranty
Low-Pressure PU Foaming Machine for Medical Polyurethane Sponge

Product Overview

Specially designed for precision pouring of medical polyurethane sponge, stably producing wound dressings, medical pads, hemostatic sponges and other medical consumables.

This low-pressure PU dispensing machine can be evaluated for sponge formulations intended for medical applications. Metering, mixing, temperature control and cleaning arrangements are selected around the material and production brief. Medical-use suitability, biocompatibility, contamination control and sterilization require separate validation of the formulation, finished device and manufacturing process. Equipment supply does not establish a sterile production environment or medical-product approval.

Product Overview

Configured

To Your Production Brief

Operation Workflow

Material Preparation

Select the formulation and establish controlled handling and cleaning procedures for the intended sponge application.

Temperature and Recipe Setting

Confirm the material temperatures, tank arrangement and mixing ratio with the formulation supplier.

Metering and Mixing Trials

Verify dispensing repeatability and mixing quality on the selected formulation and operating range.

Molding and Finished-Part Validation

Mold representative specimens and validate absorption, contamination control and any intended medical-use requirements separately.

HF-Sponge-1A1B-MedicalSponge

Technical Specifications

Standard configuration parameters for the medical sponge PU foam pouring machine. Customizations including tank capacity are available upon request.

Technical ParameterHF-Sponge-1A1B-Medical Sponge
Pouring Rate50–1000 g/s
Raw Material RatioMedical‑grade polyether polyol : Medical‑grade isocyanate (MDI) = 100:85–95
Tank Capacity (Optional)100 / 150 L
Mixing Head Speed5000–9000 r/min
Dynamic Metering Accuracy≤±0.3% (Full range)
Tank Configuration1A1B two‑component independent temperature control
Material Temperature Control (Tank A)25–45℃
Material Temperature Control (Tank B)20–40℃
Foaming Pressure0.5–2.0 MPa
Cleaning SystemConfigured circulation cleaning and air purge; cleaning and contamination-control procedures require validation for the intended application.
Power5.5–8 kW
Control SystemPLC + touch screen + multi‑formula storage
Warranty1 year
CertificationsConfirm applicable documents for the quoted configuration
WHY CHOOSE US

Key Features & Advantages

Engineered for sterility, biocompatibility, and precision in medical sponge manufacturing.

Configured Material Handling

Confirm tank arrangement, material-contact construction and cleaning requirements in the equipment specification.

Temperature and Metering Control

Set control requirements around the selected formulation and verify them during commissioning.

Finished-Sponge Validation

Absorption, biocompatibility and intended medical-use suitability require formulation and finished-product testing.

Applicable Documentation

Request records for the quoted equipment. Medical-product approval and quality-system certification are separate from dispensing-machine capability.

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Browse other equipment in our catalog. These listings are for product discovery; compatibility and production-line scope are confirmed separately for your material, process and output requirements.

SUPPORT

Frequently Asked Questions

Can this equipment be evaluated for sponge used in medical applications?
Yes, subject to formulation trials and a defined production scope. The intended finished device requires its own design and regulatory assessment.
Does the machine establish sterile production or biocompatibility?
No. Cleaning, contamination control, sterilization and biocompatibility require validation of the manufacturing process and finished product.
How are material changeovers assessed?
Define material compatibility, cleaning procedures and carryover acceptance criteria, then validate the procedure through representative trials.
What certification documents are available?
Request applicable records for the quoted model and configuration. Management-system certificates do not certify a medical product or establish sterile-process validation.