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DMH type dry heat sterilization box
DMH type dry heat sterilization box
Phone：+86 13813895449/+86 18851697216
Tel：025-85704510
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- Characteristic
- Parameter
- Relevant
DMH type dry heat sterilization box product usage
This series of products is mainly used for drying, sterilizing, and removing heat sources from heat-resistant items such as penicillin bottles, aluminum caps, metal vessels, and glassware in the pharmaceutical industry.
Structural characteristics
1. All parts inside the cavity that may come into contact with objects are made of 304-2B or 316L stainless steel material.
2. The outer surface is made of 304-2B stainless steel material, using a new production process that meets GMP requirements and makes the appearance more simple and beautiful.
3. Unique insulation method ensures that the surface temperature of the product is ≤ room temperature+15 ℃.
4. The inner chamber adopts TIG sealed welding method, and the four corner arc transition structure of the inner chamber body has no dead corners and is easy to clean.
5. High temperature resistant and efficient filters are installed inside the chamber for filtration.
6. The high-temperature resistant and high-efficiency filter inside the chamber adopts a double-layer flat seal with a negative pressure seal in the middle.
Technical features
1. Leading technology achieves dynamic hundred level and excellent temperature uniformity of dry heat sterilization cabinets.
2. The mobile door adopts a safe and stable pneumatic opening and closing system, and adopts advanced vacuum sealing method to ensure good sealing of the door. It is simple and practical, effectively avoiding contamination of sterilized items.
3. The inlet and exhaust systems of this series of products are equipped with H13 level high-temperature resistant and high-efficiency filters on one side of the chamber, with a filtration efficiency of 99.99%, ensuring that the chamber reaches a hundred level. The main filter of the chamber adopts an innovative combination sealing process, which effectively improves product efficiency while making disassembly and maintenance easier. The laminar flow plate inside the cavity adopts a unique hole distribution to control the horizontal laminar airflow, effectively improving the thermal energy utilization rate and temperature uniformity.
4. The equipment adopts an advanced fully automatic control system, which automatically controls the temperature and maintains a positive pressure system inside the cavity. An independent over temperature protection system effectively ensures equipment safety.
5. This product is equipped with a multifunctional verification interface for dust particle verification testing and temperature distribution testing. The main filter of the chamber is equipped with a DOP verification port.
6. Multiple cooling methods to improve work efficiency.
Equipment and Document System Standards
1. CGMP regulations
2. Pharmacopoeia of the People's Republic of China (2010 edition)
3. Good Manufacturing Practice for Drugs (2009)
4. Appendix 1, 11, and 15 of the EU GMP Guidelines
5. Federal Regulations (CFR) 21, Part 11: Electronic Records, Electronic Signature
6. Guidelines for Good Automation Production Practices (5th Edition)/Compliant with GMP5
7. ISO14644-1 (for cleanliness levels)
8. ISO14644-3 (for efficient particle integrity testing)
Verify the system
1. Imported ATI PAO tester is used for integrity testing of side high temperature and high-efficiency filters.
2. FLUKE multi-channel temperature verification instrument from the United States, providing heat distribution detection reports, thermocouple calibration reports, and FH value reports.
technical parameter：
model DMH-1 DMH-2 DMH-3 DMH-4 Studio sizemm(Width x Depth x Height) 600×500×750 800×800×1000 1000×1000×1200 1000×1200×1500 External dimensionsmm(Width x Depth x Height) 1650×900×1750 1850×1200×1950 2050×1400×2150 2050×1600×2450 heating power kw 9 15 22 28 Circulating fan powerkw 1.1 2.2 3.0 4.0 Supplement fan powerkw 0.06 0.18 0.18 0.25 Power of dehumidification fankw 0.18 0.25 0.37 0.75 Design temperature range℃ room temperature~300 room temperature~300 room temperature~300 room temperature~300 Cleanliness level 100 100 100 100 Circulating fan air volumem3/h 2540 2700 2900 3200 Supplement the air volume of the fanm3/h 300 408 408 408
Purification level：The dimensions of the 10000 level exterior are shown in the table below：
model A(width) B(deep) C(high) D(Moisture outlet) E F G M DMH-1 1350 900 1700 Φ60 180 1/2C 600 200 DMH-2 1550 1100 1950 Φ60 180 1/2C 700 220 DMH-3 1750 1300 2150 Φ60 180 1/2C 800 220 DMH-4 1750 1500 2450 Φ60 180 1/2C 800 220
DMH type dry heat sterilization box
(DATE：24-10-24 VIEW：570)
DMH type dry heat sterilization box product usage
This series of products is mainly used for drying, sterilizing, and removing heat sources from heat-resistant items such as penicillin bottles, aluminum caps, metal vessels, and glassware in the pharmaceutical industry.
Structural characteristics
1. All parts inside the cavity that may come into contact with objects are made of 304-2B or 316L stainless steel material.
2. The outer surface is made of 304-2B stainless steel material, using a new production process that meets GMP requirements and makes the appearance more simple and beautiful.
3. Unique insulation method ensures that the surface temperature of the product is ≤ room temperature+15 ℃.
4. The inner chamber adopts TIG sealed welding method, and the four corner arc transition structure of the inner chamber body has no dead corners and is easy to clean.
5. High temperature resistant and efficient filters are installed inside the chamber for filtration.
6. The high-temperature resistant and high-efficiency filter inside the chamber adopts a double-layer flat seal with a negative pressure seal in the middle.
Technical features
1. Leading technology achieves dynamic hundred level and excellent temperature uniformity of dry heat sterilization cabinets.
2. The mobile door adopts a safe and stable pneumatic opening and closing system, and adopts advanced vacuum sealing method to ensure good sealing of the door. It is simple and practical, effectively avoiding contamination of sterilized items.
3. The inlet and exhaust systems of this series of products are equipped with H13 level high-temperature resistant and high-efficiency filters on one side of the chamber, with a filtration efficiency of 99.99%, ensuring that the chamber reaches a hundred level. The main filter of the chamber adopts an innovative combination sealing process, which effectively improves product efficiency while making disassembly and maintenance easier. The laminar flow plate inside the cavity adopts a unique hole distribution to control the horizontal laminar airflow, effectively improving the thermal energy utilization rate and temperature uniformity.
4. The equipment adopts an advanced fully automatic control system, which automatically controls the temperature and maintains a positive pressure system inside the cavity. An independent over temperature protection system effectively ensures equipment safety.
5. This product is equipped with a multifunctional verification interface for dust particle verification testing and temperature distribution testing. The main filter of the chamber is equipped with a DOP verification port.
6. Multiple cooling methods to improve work efficiency.
Equipment and Document System Standards
1. CGMP regulations
2. Pharmacopoeia of the People's Republic of China (2010 edition)
3. Good Manufacturing Practice for Drugs (2009)
4. Appendix 1, 11, and 15 of the EU GMP Guidelines
5. Federal Regulations (CFR) 21, Part 11: Electronic Records, Electronic Signature
6. Guidelines for Good Automation Production Practices (5th Edition)/Compliant with GMP5
7. ISO14644-1 (for cleanliness levels)
8. ISO14644-3 (for efficient particle integrity testing)
Verify the system
1. Imported ATI PAO tester is used for integrity testing of side high temperature and high-efficiency filters.
2. FLUKE multi-channel temperature verification instrument from the United States, providing heat distribution detection reports, thermocouple calibration reports, and FH value reports.
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