Sweden

Medizinprodukt-Marktintelligenz für Sweden. Regulatorische Änderungen, Wettbewerber und Beschaffungstrends.

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153

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Neueste Signale

reg_registration2026-06-01

AB GERMA in Sweden has FDA registration under product code IKY for one listed medical device.

FDA Device Registration & Listing ·

reg_enforcement2026-05-29

A study on a plug-based device for femoral arteriotomy closure in acute type A aortic dissection surgery was completed.

ClinicalTrials.gov · 2017-01-01

mkt_event2026-05-29

The 2026 MedTech Forum in Sweden highlighted the EMA's innovative device pilot and EU's IVDR regulation.

Medical Device Network · 2026-05-29

reg_enforcement2026-05-28

The Uphold LITE system for pelvic organ prolapse has completed a safety and efficacy assessment study.

ClinicalTrials.gov · 2012-01-01

mkt_event2026-05-22

The 2026 MedTech Forum highlighted healthcare continuity and medical device supply resilience during crises in Europe.

Medical Device Network · 2026-05-22

reg_guidance2026-05-20

A study on Dermalyser's effectiveness in assessing melanoma thickness via dermoscopy is set to begin in Sweden.

ClinicalTrials.gov · 2025-01-31

reg_enforcement2026-05-15

The AFteR Registry is recruiting to monitor the Occlutech AFR device's efficacy and safety in heart failure patients.

ClinicalTrials.gov · 2020-10-28

reg_enforcement2026-05-15

The study evaluated the tolerability, safety, and performance of Bactiguard coated BIP Endotracheal tubes versus standard tubes.

ClinicalTrials.gov · 2012-04-01

reg_enforcement2026-05-12

A completed clinical investigation evaluated a topical medical device's effectiveness on itching after 3 days of use.

ClinicalTrials.gov · 2023-01-30

reg_registration2026-05-12

Naslund Medical AB has registered a medical device with the FDA under product code IYE.

FDA Device Registration & Listing ·

reg_enforcement2026-05-08

The Navina Mini study completed with 40 subjects in Sweden for low-volume transanal irrigation over four weeks.

ClinicalTrials.gov · 2024-01-18

reg_enforcement2026-05-07

The Endodrill Model X biopsy instrument was evaluated for safety and efficacy against standard methods in Sweden.

ClinicalTrials.gov · 2020-09-30

com_launch2026-05-05

A multicenter study evaluates a wearable stroke indication system for patients with recent TIA or minor strokes.

ClinicalTrials.gov · 2022-01-01

reg_registration2026-05-05

Philips Ultrasound LLC registered the Extended Compact Cart as a Class I medical device in EUDAMED.

EUDAMED EU Device Database ·

reg_registration2026-05-05

SWEDEN & MARTINA S.p.A. has FDA registration for 2 medical devices under product code DZE.

FDA Device Registration & Listing ·

reg_enforcement2026-05-04

The clinical investigation confirmed the safety and performance of MINIVISC® PLUS for various eye surgeries.

ClinicalTrials.gov · 2024-02-20

reg_enforcement2026-05-04

A completed study evaluated a plug-based arteriotomy closure device in minimally invasive mitral valve surgery.

ClinicalTrials.gov · 2016-02-01

com_launch2026-05-02

Carponovum AB developed a novel adaptive anastomotic method to improve colorectal surgery outcomes and reduce leakage risks.

ClinicalTrials.gov · 2021-04-01

reg_enforcement2026-05-02

The study evaluates FeNO's role in diagnosing asthma in patients with prolonged respiratory symptoms using the NIOX MINO® device.

ClinicalTrials.gov · 2011-11-01

mkt_report2026-05-02

A study completed by Uppsala University Hospital evaluated a new device's impact on IV catheter complications.

ClinicalTrials.gov · 2023-05-04

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