Medical Products
Molded fiber packaging used in the medical sector plays an important role in the safety and environmental sustainability of products.
This packaging solution offers a reliable and environmentally friendly option, in line with the needs of the industry.
These products offer healthcare professionals and patients a safe, hygienic and personalized experience.
Kidney Bowl
- Product Size (mm): 150x255x45
- For the transport of human waste and other substances at temperatures up to -35 degrees centigrade (+/-).
- It can also be used to hold syringes and dressings for up to 4 hours.
- According to the classification provisions of Rule 1 of Annex VIII of EU Regulation 2017/745, our products are classified as Class I Medical Devices.
- Declaration of Conformity has been prepared according to MDR 2017/745 Annex IV.
- ISO 13485:2016
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Bedpan
- Product Size (mm): 353x287x75
- For the transport of human waste and other substances at temperatures up to -35 degrees centigrade (+/-).
- It can also be used to hold syringes and dressings for up to 4 hours.
- According to the classification provisions of Rule 1 of Annex VIII of EU Regulation 2017/745, our products are classified as Class I Medical Devices.
- Declaration of Conformity has been prepared according to MDR 2017/745 Annex IV.
- ISO 13485:2016
Click for details
Kidney Bowl
Product Size (mm): 150x255x45. For the transport of human waste and other substances at temperatures up to -35 degrees centigrade (+/-). It can also be used to hold syringes and dressings for up to 4 hours. According to the classification provisions of Rule 1 of Annex VIII of EU Regulation 2017/745, our products are classified as Class I Medical Devices. Declaration of Conformity has been prepared according to MDR 2017/745 Annex IV. ISO 13485:2016.
Detaylar için tıklayınız
Bedpan
Product Size (mm): 353x287x75. For the transport of human waste and other substances at temperatures up to -35 degrees centigrade (+/-). It can also be used to hold syringes and dressings for up to 4 hours. According to the classification provisions of Rule 1 of Annex VIII of EU Regulation 2017/745, our products are classified as Class I Medical Devices. Declaration of Conformity has been prepared according to MDR 2017/745 Annex IV. ISO 13485:2016.
Detaylar için tıklayınız
