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We reviewed 3 live results for medical devices 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, ER7232PLUS - PRYTIME MEDICAL - Prytime Medical Devices Inc. ER-REBOA Plus Balloon Occlusion Catheter, (BX/1) and CARDIAC PACEMAKERS & DEVICES.
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: KAPTAN SCIENTIFIC, INC.
Description
The Prytime Medical Devices Inc. ER-REBOA Plus Balloon Occlusion Catheter (model ER7232PLUS) is a medical balloon catheter item packaged as a single-count box (BX/1). Offered via Kaptan Scientific as an in-stock stock item with an expiry date of August 23, 2026, it is sold as-is without returns or refunds. If expired, it is not for patient use and is restricted to research, veterinary, or educational applications per applicable regulations.
Best for
medical professionals, researchers, balloon occlusion procedures and medical research
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Source: The Harley Street Heart & Vascular Centre
Description
The Harley Street Heart & Vascular Centre in Singapore provides comprehensive cardiac pacemaker and implantable cardiac device healthcare services. Offerings include permanent pacemaker (PPM) insertion, implantable cardioverter-defibrillator (ICD) insertion, and implantable loop recorder (ILR) insertion, along with dedicated device checks, clinical follow-up, and remote home monitoring to treat heart failure and manage slow or irregular heart rhythm disorders.
Best for
patients with slow or irregular heartbeats, heart failure patients, pacemaker and cardiac device implantation and routine device follow-up and checks
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| Compare | #1Medical Devices – EU MDR Certification (EU) 2017/745 | #2ER7232PLUS - PRYTIME MEDICAL - Prytime Medical Devices Inc. ER-REBOA Plus Balloon Occlusion Catheter, (BX/1) | #3CARDIAC PACEMAKERS & DEVICES |
|---|---|---|---|
| Source | SZUTEST | KAPTAN SCIENTIFIC, INC. | The Harley Street Heart & Vascular Centre |
| 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. | The Prytime Medical Devices Inc. ER-REBOA Plus Balloon Occlusion Catheter (model ER7232PLUS) is a medical balloon catheter item packaged as a single-count box (BX/1). Offered via Kaptan Scientific as an in-stock stock item with an expiry date of August 23, 2026, it is sold as-is without returns or refunds. If expired, it is not for patient use and is restricted to research, veterinary, or educational applications per applicable regulations. | The Harley Street Heart & Vascular Centre in Singapore provides comprehensive cardiac pacemaker and implantable cardiac device healthcare services. Offerings include permanent pacemaker (PPM) insertion, implantable cardioverter-defibrillator (ICD) insertion, and implantable loop recorder (ILR) insertion, along with dedicated device checks, clinical follow-up, and remote home monitoring to treat heart failure and manage slow or irregular heart rhythm disorders. |
| Best for | medical device manufacturers, regulatory affairs specialists, obtaining EU MDR CE certification and demonstrating European medical device compliance | medical professionals, researchers, balloon occlusion procedures and medical research | patients with slow or irregular heartbeats, heart failure patients, pacemaker and cardiac device implantation and routine device follow-up and checks |
| Action | SZUTEST | KAPTAN SCIENTIFIC, INC. | The Harley Street Heart & Vascular Centre |
| Rate this product |
"Medical Devices – EU MDR Certification (EU) 2017/745 from SZUTEST."
Note: TopFind AI compiles product and service information for general comparison purposes only.