AZR MEDICAL Company Brand Name

PE Pouch & Dialysis Paper Patched-PE Pouch

Product Information

ParameterDetails
MaterialMedical-grade PE material(LDPE, HDPE, LLDPE)
ColorTranparent or custom colors
ThicknessCustom
SizeCustom
Printing methodFlexographic printing
Printingcustom (color: up to 4)
Seal TypeHeat sealed
Sterilization method EO, Irradiation, Gamma-ray
Test ReportBiocompatibility test (based on ISO10993)
accelerat aging test, vaccum leakage test, seal peeling test (based on ASTM F 1980-07)
Shelf Life24 months from manufacture date

Features

  • Strong heat sealing and clean appearance
  • Dialysis Paper-Patched PE Pouch laminated with medical dialysis paper, allowing effective EO gas sterilization while maintaining a strong bacterial barrier
  • Transparent PE film: easy to identify internal product
  • Moisture-proof: Standard PE Pouch ideal for non-sterile and secondary medical packaging
  • Stretch-resistant: Suitable for long-distance transportation. The bag body is not prone to damage, thus preventing the internal products from being contaminated
  • Low-temperature performance: brittleness is not likely to occur under freezing conditions.

Applications

  • Suitable for syringes, tubing, catheters, infusion sets etc low-risk sterile medical consumables
  • Primary packaging and secondary packaging

Our Custom Capability

  • Size: length between 30~650mm, width between 30~450mm (tolerance: ±2mm)
  • Thickness: single layer 0.03~0.25mm (tolerance: ±3μm)
  • Bag color
  • Printing design
  • Tear line shape
  • Light-proof pouch
  • Irradiable bags/Electron beam sterilization bag
  • …… Other custom options according to custoner’s specific requirements

Medical Waste Biohazard Bag

Product information

ParameterDetails
MaterialLDPE / HDPE / PP
ColorYellow (infectious waste), Red (biohazard), Black (general medical waste)
Thickness30–100 microns (customizable)
Size300×400mm to 950×1250mm (custom sizes available)
Tolerable temperaturePE–121℃, PP–135℃
PrintingBiohazard symbol + Warning text, up to 3 colors flexographic printing
Seal TypeFlat / Drawstring / Self adhesive
CertificationISO 9001, ISO 13485, ISO 11607 compliant
Shelf Life36 months from manufacture date

Key Features

  • Puncture & Tear Resistant — High-strength resin blend prevents sharp waste from piercing the bag wall
  • Leak-Proof Seal — Uniform heat-sealed seams tested to withstand liquid loads without failure
  • Universal Biohazard Marking — Pre-printed biohazard symbol and bilingual warning text for regulatory compliance
  • Color-Coded System — Available in standard medical waste colors to support waste segregation protocols
  • Custom Branding — Logo printing and custom warning text available upon request
  • Cleanroom Manufactured — Produced in controlled environment to prevent contamination of waste collection materials

Kraft Paper Sterilization Pouch

The Kraft Sterilization Pouch is constructed from 100% pure 60g kraft paper. This heavy-duty kraft paper provides excellent tear and puncture resistance, making it ideal for packaging heavy, sharp, or irregularly shaped surgical instruments.

Product information

  • Material: 60g Pure Kraft Paper
  • High temperature resistant–from 160℃~220℃
  • Dry Heat, Steam and EO sterilization compatible
  • Shelf life: 3 years

Custom Options

  • Size
  • Logo printing
  • Paper color
  • Packaging method

Key Features

  • Excellent tear and puncture resistance
  • Ideal for manicure or tattoo instruments
  • Self adhesive–easy and hygienic to use
  • Environmentally friendly

Size Specifications

ITEM NO SIZES (mm) Actual Inner Size (mm) PACK (PCS/CARTON)
KF-75180 75×180 60*153 10000
KF-100230 100×230 80*200 8000
KF-130230 130×230 110*200 8000

Chemical Indicator Strips

Product information

  • Material: Ink made from chemical substances, colorants and their additives+medical special card paper.
  • Application: hospitals, pharmacies, and dental clinics, pet hospitals, food processing, beverage,dairy processing, health products, Laboratory, medical research institute,Health prevention and disinfection service institution etc.
  • Complies with ISO 11140-1, EN 867-4 and ISO 11140-4

Sterilization Process

  • 1. Place the plasma sterilization indicator strip at the center of the standard test package or the item itself, with the end of the card marked with the indicator facing down. Put it in the middle of the item package or in the area that is the most difficult to sterilize.
  • 2. According to the routine of sterilization operations, after a sterilization cycle under a temperature of 50°C – 60°C, with a concentration of 60% hydrogen peroxide solution at 2.3mg/L, the color block of the indicator card changes from green to yellow, which indicates that the sterilization package has undergone sterilization treatment; if the color change of the indicator card is uneven or there is no color change, it indicates that this package has not undergone sterilization treatment.

Notes for Attention

  •  The indicator strips must not come into contact with acidic or alkaline substances during storage and use.
  • Avoid moisture (relative humidity should be less than 50%), store away from light, and protect from ultraviolet fluorescent lamps and sunlight.
  • Store in a dark place, at room temperature, with ventilation, in a dry environment, and sealed.

Chemical Indicator Tapes

Product Information

Our factory chemical indicator tapes are the ideal and safe solution for closing all wrapping materials. They are constructed from pressure semi-crepe paper which on one side is the adhesive glue and the other side is indicator strip are printed. The process indicator ink shows an easy and accurate color change and indicates if the pack has been processed.

Sterilization color change

EO–from red to green, STEAM–from beige to black, Plasma–from blue to red.

Key Features

  • Pressure-sensitive adhesive, with excellent adhesion and good sealing and packaging function;
  • The waterproof layer does not tend to loosen or break when heated;
  • The water-reactive fuel is not easily damaged when exposed to water, and its color does not fade easily after sterilization;
  • Remove the packaging from the sterilizer without leaving any residue.

Size Specifications

DESCRIPTIONITEM NOSIZEPACK (PCS/CTN)
Steam Indicator TapeST-125012mm×50m76rolls/ctn
Steam Indicator TapeST-195019mm×50m48rolls/ctn
Steam Indicator TapeST-255025mm×50m36rolls/ctn
EtO Indicator TapeET-125012mm×50m76rolls/ctn
EtO Indicator TapeET-195019mm×50m48rolls/ctn
EtO Indicator TapeET-255025mm×50m36rolls/ctn
Plasma Indicator TapePT-125012mm×50m76rolls/ctn
Plasma Indicator TapePT-195019mm×50m48rolls/ctn
Plasma Indicator TapePT-255025mm×50m36rolls/ctn
 

Bowie-Dick Test Pack / Paper

Product information

  • Material: B-D test paper, laminated sheets, laminated sheets with backing, foam sheets, and a sheet of cellophane wrapped around it, which is then sealed and packaged with an instruction label.
  • Usage: determining the effect after the installation and commissioning of new sterilizers, and measuring the performance after the maintenance of sterilizers.
  • Application: Suitable for Medical, Dental, Eye Center, Laboratory, Surgical Center, Pharmaceutical, and Pet Hospital, Biotechnology industry, Biomedical field; zoology research institute; biological laboratory.
  • Pre-assembled disposable Bowie-Dick test pack for detection of defects in the sterilization process
  • Easy-to-read test sheet with detailed instructions for use and interpretations of results
  • Complies with ISO 11140-1, EN 867-4 and ISO 11140-4

Sterilization Process

The pattern on the B-D test paper will turn into a uniform dark brown to black when the sterilizer operates at 132℃ ~134℃ for 3.5 minutes. If the cold air is not completely expelled, the cold air inside the package will affect the penetration of the steam, resulting in a lighter-colored area in the center of the B-D test paper that is different from the surrounding areas.

Notes for Attention

  • The test patterns inside the BD test kit must not come into contact with acidic or alkaline substances during storage and use.
  • Avoid moisture (relative humidity should be less than 50%), store away from light, and protect from ultraviolet fluorescent lamps and sunlight.
  • The test shall be conducted under steam conditions at 132~134℃ for no more than 4 minutes. The test shall be conducted in an empty autoclave before the first sterilization of the day.
  • This product cannot be used to test the effectiveness of pressure steam sterilization.