Data / Medical devices / Netherlands / Ceva Logistics Netherlands B.V.

Ceva Logistics Netherlands B.V.: FDA-registered device maker in Oostrum Limburg, Netherlands, 3 510(k) clearances

Name: Ceva Logistics Netherlands B.V. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Ceva Logistics Netherlands B.V. is registered with the FDA (registration 3012907824) in Oostrum Limburg, Netherlands. It lists 18 device types. The FDA files 3 510(k) clearances under its listings, the newest dated January 26, 2015. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3012907824
Address: bellstraat 20, Oostrum Limburg, Netherlands, 5807GE
Owner or operator: CEVA Logistics (10051642)
Roles: Exporter to the US, Repackager or relabeler
First device listed: April 15, 2016
Registered through: 2026
Brand names listed: BSN Medical

Devices it lists

Device	Product code	Class	Role	Source
Bandage, Cast	ITG	1	Repackager or relabeler	accessdata.fda.gov
Bandage, Elastic	FQM	1	Exporter to the US, Repackager or relabeler	accessdata.fda.gov
Bandage, Liquid, Skin Protectant	NEC	1	Repackager or relabeler	accessdata.fda.gov
Binder, Medical, Therapeutic	MDR	1	Repackager or relabeler	accessdata.fda.gov
Dressing, Wound, Drug	FRO	U	Repackager or relabeler	accessdata.fda.gov
Dressing, Wound, Hydrogel Without Drug And/Or Biologic	NAE	1	Repackager or relabeler	accessdata.fda.gov
Dressing, Wound, Hydrophilic	NAC	1	Repackager or relabeler	accessdata.fda.gov
Dressing, Wound, Occlusive	NAD	1	Repackager or relabeler	accessdata.fda.gov
Gauze / Sponge,Nonresorbable For External Use	NAB	1	Repackager or relabeler	accessdata.fda.gov
Joint, Ankle, External Brace	ITW	1	Repackager or relabeler	accessdata.fda.gov
Joint, Knee, External Brace	ITQ	1	Repackager or relabeler	accessdata.fda.gov
Orthosis, Cervical	IQK	1	Repackager or relabeler	accessdata.fda.gov
Orthosis, Limb Brace	IQI	1	Repackager or relabeler	accessdata.fda.gov
Orthosis, Lumbar	IQE	1	Repackager or relabeler	accessdata.fda.gov
Sling, Arm	ILI	1	Repackager or relabeler	accessdata.fda.gov
Splint, Extremity, Non-Inflatable, External, Non-Sterile	NOC	1	Repackager or relabeler	accessdata.fda.gov
Support, Arm	IOY	1	Repackager or relabeler	accessdata.fda.gov
Tape And Bandage, Adhesive	KGX	1	Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
January 26, 2015	K143151	Cutimed Sorbact Wound Dressings (Cutimed Sorbact Hydroactive, Cutimed Sorbact Hydroactive B, Cutimed Siltec Sorbact)	FRO	Substantially Equivalent	Bsn Medical GmbH	accessdata.fda.gov
January 24, 2011	K100591	SORBACT	FRO	Substantially Equivalent	Abigo Medical AB	accessdata.fda.gov
April 19, 2007	K063059	SORBACT WOUND DRESSING	FRO	Substantially Equivalent	Abigo Medical AB	accessdata.fda.gov

Compare with other makers

Updated January 26, 2015. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.