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STEP
1 |
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To produce high
quality products requires stringent
quality control systems on the
incoming raw materials. Various
testing and research have been
implemented to ensure our
manufacturing processes are only
using the right specification and
high quality raw materials to
produce the tip-top quality finished
products. |
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STEP
2 |
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The dipping
process is including optimum control
on the temperatures, duration of
dipping, viscosity flow of
compounded latex, effective leaching
process which eventually produced
intact latex films that are
impermeable to viruses and with high
elasticity and durability
properties. |
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STEP
3 |
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The parameters
control systems for the raw
materials used and operational
process are set up to conform to the
relevant or specific sections of the
USA FDA's Good Manufacturing
Practices (GMP), ISO 9001:2000, ASTM
& EN455 Standards. With different
formulations, a range of natural
latex and Nitrile gloves are
produced to pass the
Biocompatibility tests which
included the Delayed Contact
Sensitization and Primary Skin
Irritation Studies, Dermal
Observation and the Cytoxicity Test.
We will make sure Flexitech gloves
are safe for the users. The 100%
consumer's safety is always our main
concerns. |
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STEP
4 |
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The Performance
Properties are guaranteed by
eliminating pinholes gloves with a
fully automatic Watertight Testing
machine which is calibrated to fill
gloves with 1,000ml of water at
least 2 minutes in according to the
Sampling Plan Special Inspection
Level S-4, AQL 1.5. |
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STEP
5 |
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Both the
prepowered and powdefree latex
examination gloves are produced
within the USA ASTM permissible
low-protein level while the
protein-free Nitrile gloves are low
modulus with high puncture and
abrasion resistance which are
extensively used in Healthcare,
Clean room and Household industries. |
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STEP
6 |
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After the final
random QA inspection, different
types of finished good are pack
flat-stack into dispenser boxes and
cartons in different hygienically
controlled environments. |
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