SKYLLA EUROPE BV

FDA Device Registration & Listing · Geleen Limburg, NL · Registration 3016661700

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3016661700
FEI Number
3016661700
Entity Name
SKYLLA EUROPE BV
City/State/Country
Geleen Limburg, NL
Establishment Address
Tomeikerweg, 10, Geleen Limburg 6161 RB, NL
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Skylla Europe BV (Owner Number: 10086652)
Owner / Operator Contact Address
Tomeikerweg, 10, Geleen, NL-LI 6161 RB, NL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMR Device, Transfer, Patient, Manual General Hospital Class 1 880.6785 2022-11-29

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Skylla Europe BV
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3036731074 Skylla Morocco Sarl Kenitra, MA
3025355675 Skylla SARL Aissa Tunis, TN

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016661700. Last updated year: 2026. Please use registration number 3016661700 when referencing this establishment in official correspondence.
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