Spetec cleanroom system
The Spetec cleanroom system is a state-of-the-art solution for maintaining particle-free and sterile conditions in cleanrooms. These systems are particularly important in industries such as semiconductor manufacturing, precision mechanics, optics and optoelectronics, laser technology and food production. Spetec's cleanroom equipment is characterized by its robust design and antimicrobial, corrosion-resistant surfaces, which ensure optimum protection for employees and products. Similar to the Spetec stainless steel cleanroom cell, the Spetec cleanroom system offers a reliable solution for demanding cleanroom requirements.
Technical details and functions
The Spetec Cleanroom System includes a variety of equipment and services specifically designed to maintain and verify cleanroom conditions. Here are some of the key technical details and features:
-
Particle counting: regular checks of the number of particles in the air to ensure that cleanroom conditions are maintained.
-
Filter change for laminar flow boxes (LF unit): Replacement of filters of different makes to ensure continuous air cleanliness.
-
Leak detection and elimination: Identifying and fixing leaks to maintain the integrity of the cleanroom.
-
Volume flow rate determination or flow velocity: Measurement of the air flow to ensure uniform distribution of air in the cleanroom.
-
Temperature and relative humidity measurement: Monitoring of ambient conditions to ensure optimum working conditions.
-
HEPA filter/filter system installation check: Ensuring the correct installation and function of HEPA filters.
-
DEHS leak test: Performing leak tests with DEHS (Di-Ethyl-Hexyl-Sebacat) to check the tightness of the system.
-
Cleanroom validation and certification in accordance with EN ISO 14644 and GMP guidelines: recording and confirmation of the measurement parameters specified in DIN EN ISO 14644.
Certifications and standards
The Spetec cleanroom system complies with all relevant national and international standards and guidelines, including
- ENISO 14644: This standard specifies the requirements for air cleanliness in cleanrooms.
-
GMP guidelines: Good Manufacturing Practice for the production of pharmaceuticals and active pharmaceutical ingredients.
-
VDI 2083: Guidelines for cleanrooms and associated cleanroom areas.
-
US Fed Std. 209E: American standard for the classification of air cleanliness in cleanrooms.
Application examples
The Spetec cleanroom system is used in various highly sensitive production environments, including
-
Semiconductor manufacturing: ensuring a particle-free environment for the production of microchips.
-
Precision mechanics and optics: Avoiding contamination in the production of precision instruments and optical components.
-
Laser technology: ensuring a clean environment for the manufacture and maintenance of laser systems.
-
Food production: Maintaining hygienic conditions to prevent contamination.
FAQs
How often should the filters in the Spetec cleanroom system be changed?
Filters should be checked regularly and changed at least once a year depending on usage and environment. More frequent filter changes may be necessary if the particle load in the environment is high.
What certifications does Spetec offer for cleanrooms?
Spetec offers certifications according to EN ISO 14644 and GMP guidelines. These certifications include the recording and confirmation of all relevant measurement parameters such as particle count and flow velocity.
Can the Spetec cleanroom system be retrofitted in existing cleanrooms?
Yes, the Spetec cleanroom system can be integrated and retrofitted into existing cleanrooms. Our experts offer comprehensive advice and support during installation and maintenance.
Conclusion
The Spetec cleanroom system offers a comprehensive solution for maintaining sterile and particle-free conditions in various industries. With robust materials, antimicrobial surfaces and comprehensive services such as particle counting and filter replacement, Spetec ensures that your cleanrooms always meet the highest standards. Similar to the Spetec cleanroom cell, the Spetec cleanroom system offers a reliable and efficient solution for demanding cleanroom requirements.
| Cleanroom equipment: |
Clean room cell |
Spetec Clean room technology Service
We - as a manufacturer and service provider for clean room technology - provide a range of device variants on the one hand, and fast and universal service assistance on the other hand. Now we have used our many years of experience as a manufacturer to develop a services offering, which allows us to test, service, and maintain your clean room system using state of the art measuring equipment.
Very clean air is not just vital in clinic operating rooms. Highly sensitive production environments, such as those in the semiconductor production, precision engineering, optics and optoelectronics, laser technology, or food processing industries, also demand a sufficient level of ambient air quality. In order to ensure this, flow velocity or filter tests are required at regular intervals.
We offer the following services:
- Particle counts
- Replacing filters in various brands of laminar flow boxes (LF units)
- Finding and fixing leaks
- Determining volume flow rates or flow velocities
- Temperature and relative humidity measurements
-HEPA filter / filter system installation monitoring
- DEHS leak test
- Clean room validation and certification in accordance with EN ISO 14644 and GMP guidelines
We also perform certification within the framework of EN ISO 14644, that is, we record the measurement parameters defined in DIN EN ISO 14644 such as particle counts, flow velocities, etc. All of these parameters are confirmed with a corresponding certificate.
All of the particle measurement devices, air speed, temperature, and humidity sensors we use are tested and calibrated every 12 months.
Our offering includes service and maintenance work as well as certification of clean rooms and laminar flow boxes according to the current national and international guidelines and standards. These include the VDI 2083 and DIN EN ISO 14644 guidelines as well as the US Fed Std. 209E. You receive comprehensive documentation about the measurements and a risk assessment.
Toller Kundenservice und schnelle Beantwortung aller Fragen. Wir benötigten eine komplette Laborausstattung für unseren neuen Standort. Das Team von MedSolut hat alles zu unserer Zufriedenheit geregelt.
Kunde
There are no reviews yet.
