Sueddeutsche Feinmechanik GmbH
- Business Type : Manufacturer
- Location : Germany
- Main Products : Epidural Needle,Pencil Point Or Quincke Spinal Needle, Thermolesion Needle,Seldinger Needle,Split Cannulae,Huber Needles,Applicator Needle,Brachytherapy Needles, Veterinary Cannulae,Injection Cannula In Accordance With TRBA 250, Huber Cannula In Accordance With TRBA 250, Biopsy Products,Epidural Set,Dispensing Pin,Double-ended Needle, Transfer Systems And Sets, Sterile Extraction Filter, Bottle Needles,N,
- Country/Region : Germany
- Links : Germany Health & Medicines, Germany Animal & Veterinary, Germany Veterinary Instrument,
Company Introduction
Our Locations:
The SFM headquarters are located in Waechtersbach, Germany. It is here that the largest production capacities, administration and our research and development department can be found.
Production steps:
product development, metal processing, assembly, coating, synthetic injection moulding, packaging, ETO sterilisation
Prague, Czech Republic
SFM's subsidiary SaFeMed is based in Prague-Satalice.
Production steps:
assembly, packaging
High-quality work based on consistency and transparency
We at SFM have committed ourselves to quality. This goes far beyond legal regulations and specified standards for quality assurance. For exactly this reason, we adhere particularly strictly to the stipulated rules, the obligation to provide evidence and documentation as well as transparency. SFM quality systems are permanently improved and optimised by internal and external audits.
SFM Quality Management, national and EU
Our quality management encompasses the compliance with
medical devices standard DIN EN ISO 13485:2003
the requirements of 93/42/EEC
all legal regulations of national law
which are deduced from this EU guideline, in particular
the Medizinproduktegesetz (German Medical Devices Act)
the Medizinprodukte-Verordnung (German Medical Devices Ordinance)
the Medizinprodukte-Sicherheitsplanverordnung (German Ordinance on Medical Devices Vigilance)
SFM Quality Management, Intercontinental
Furthermore, the following requirements are fulfilled:
Canadian Medical Devices Requirements
US FDA/GMP Requirements
Australian Regulatory Guidelines and Standards for Medical Devices
SFM Quality Assurance
All processes required for the manufacturing of SFM's products are monitored by a systematically implemented quality assurance system. For that purpose, SFM has an in-house physical and microbiological quality laboratory at its disposal.
If required, external laboratories are also consulted.
Another important goal of our QA system is to integrate quality- and function-relevant design specifications into the product development as early as possible.
The quality of the products and the reliability of the services is the sum of the responsibility of all our employees.
The SFM headquarters are located in Waechtersbach, Germany. It is here that the largest production capacities, administration and our research and development department can be found.
Production steps:
product development, metal processing, assembly, coating, synthetic injection moulding, packaging, ETO sterilisation
Prague, Czech Republic
SFM's subsidiary SaFeMed is based in Prague-Satalice.
Production steps:
assembly, packaging
High-quality work based on consistency and transparency
We at SFM have committed ourselves to quality. This goes far beyond legal regulations and specified standards for quality assurance. For exactly this reason, we adhere particularly strictly to the stipulated rules, the obligation to provide evidence and documentation as well as transparency. SFM quality systems are permanently improved and optimised by internal and external audits.
SFM Quality Management, national and EU
Our quality management encompasses the compliance with
medical devices standard DIN EN ISO 13485:2003
the requirements of 93/42/EEC
all legal regulations of national law
which are deduced from this EU guideline, in particular
the Medizinproduktegesetz (German Medical Devices Act)
the Medizinprodukte-Verordnung (German Medical Devices Ordinance)
the Medizinprodukte-Sicherheitsplanverordnung (German Ordinance on Medical Devices Vigilance)
SFM Quality Management, Intercontinental
Furthermore, the following requirements are fulfilled:
Canadian Medical Devices Requirements
US FDA/GMP Requirements
Australian Regulatory Guidelines and Standards for Medical Devices
SFM Quality Assurance
All processes required for the manufacturing of SFM's products are monitored by a systematically implemented quality assurance system. For that purpose, SFM has an in-house physical and microbiological quality laboratory at its disposal.
If required, external laboratories are also consulted.
Another important goal of our QA system is to integrate quality- and function-relevant design specifications into the product development as early as possible.
The quality of the products and the reliability of the services is the sum of the responsibility of all our employees.
Contact Information
- Contact Person : Mr. Albert Busch
- Telephone : 49-6053-8050
- Fax Number : 49
- Address : Brueckenstrasse 5
- Fax : 49
- Zip/Post Code : 63607
- Website : Visit website
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