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We reviewed 12 live results for eu mdr 2017 745 and narrowed them down to the 3 options that look most worth comparing first.
The options are Medical Devices – EU MDR Certification (EU) 2017/745, EU PROST and UDEM Adriatic D.O.O..
Source: SZUTEST
Description
SZUTEST GmbH provides EU MDR conformity assessment and CE marking certification under Regulation (EU) 2017/745 for medical device manufacturers. Designated as Notified Body 2975 by ZLG and the European Commission, the organization conducts conformity assessments across Class Is, Im, Ir, IIa, IIb, and Class III devices. Services include technical documentation evaluation, General Safety and Performance Requirements review, ISO 13485 quality management system certification, and laboratory testing including biomechanical implant and cybersecurity testing.
Best for
medical device manufacturers, regulatory affairs specialists, obtaining EU MDR CE certification and demonstrating European medical device compliance
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Source: BeC Natura
Description
BeC Natura EU PROST is a dietary supplement in vegetable gelatin capsules formulated to support the genitourinary system and prostate health. Its plant-based formula features Graminex G63 flower pollen extract, saw palmetto, nettle root, cranberry, pumpkin seed extract, and essential oils of lemon, sage, and juniper, enriched with vitamins C, E, B6, zinc, copper, and selenium. Suitable for vegetarian and vegan diets, EU PROST is gluten-free, sugar-free, and contains no added salt.
Best for
Men seeking prostate and urinary tract health support, Vegetarians and vegans, Daily prostate maintenance and Genitourinary system wellness
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Source: Unknown source
Description
UDEM Adriatic d.o.o. is a Croatian notified body and conformity assessment organization based in Zagreb, established in 2015. Designated as Notified Body 2696 under Regulation (EU) 2017/745 on medical devices (MDR) and accredited by the Croatian Accreditation Agency, the company provides system certification services including ISO 9001 and ISO 13485, alongside CE marking compliance assessments under the Medical Devices Regulation and Machinery Directive.
Best for
Medical device manufacturers, Machinery manufacturers, Medical device CE marking under EU MDR 2017/745 and ISO 13485 medical device quality management certification
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| Compare | #1Medical Devices – EU MDR Certification (EU) 2017/745 | #2EU PROST | #3UDEM Adriatic D.O.O. |
|---|---|---|---|
| Source | SZUTEST | BeC Natura | Unknown source |
| Description | SZUTEST GmbH provides EU MDR conformity assessment and CE marking certification under Regulation (EU) 2017/745 for medical device manufacturers. Designated as Notified Body 2975 by ZLG and the European Commission, the organization conducts conformity assessments across Class Is, Im, Ir, IIa, IIb, and Class III devices. Services include technical documentation evaluation, General Safety and Performance Requirements review, ISO 13485 quality management system certification, and laboratory testing including biomechanical implant and cybersecurity testing. | BeC Natura EU PROST is a dietary supplement in vegetable gelatin capsules formulated to support the genitourinary system and prostate health. Its plant-based formula features Graminex G63 flower pollen extract, saw palmetto, nettle root, cranberry, pumpkin seed extract, and essential oils of lemon, sage, and juniper, enriched with vitamins C, E, B6, zinc, copper, and selenium. Suitable for vegetarian and vegan diets, EU PROST is gluten-free, sugar-free, and contains no added salt. | UDEM Adriatic d.o.o. is a Croatian notified body and conformity assessment organization based in Zagreb, established in 2015. Designated as Notified Body 2696 under Regulation (EU) 2017/745 on medical devices (MDR) and accredited by the Croatian Accreditation Agency, the company provides system certification services including ISO 9001 and ISO 13485, alongside CE marking compliance assessments under the Medical Devices Regulation and Machinery Directive. |
| Best for | medical device manufacturers, regulatory affairs specialists, obtaining EU MDR CE certification and demonstrating European medical device compliance | Men seeking prostate and urinary tract health support, Vegetarians and vegans, Daily prostate maintenance and Genitourinary system wellness | Medical device manufacturers, Machinery manufacturers, Medical device CE marking under EU MDR 2017/745 and ISO 13485 medical device quality management certification |
| Action | SZUTEST | BeC Natura | UDEM Adriatic D.O.O. |
| Rate this product |
"Medical Devices – EU MDR Certification (EU) 2017/745 from SZUTEST."
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