SPARK HOLLAND BV.

FDA Device Registration & Listing · EMMEN Drenthe, NL · Registration 3006397327

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
3006397327
FEI Number
3006397327
Entity Name
SPARK HOLLAND BV.
City/State/Country
EMMEN Drenthe, NL
Establishment Address
Waanderweg 40, EMMEN Drenthe 7812 HZ, NL
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
SPARK HOLLAND BV. (Owner Number: 9096620)
Owner / Operator Contact Address
Waanderweg 40, --, EMMEN, NL-NOTA 7812 HZ, NL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

UHPLC Online SPE cartridges Online SPE Manager

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DPM Columns, Liquid Chromatography Clinical Chemistry Class 1 862.2260 2012-11-09
KIE Apparatus, High Pressure Liquid Chromatography Clinical Chemistry Class 1 862.2260 2007-01-12

Official Correspondent

Henri-Paul Karman

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

SPARK HOLLAND BV.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006397327. Last updated year: 2026. Please use registration number 3006397327 when referencing this establishment in official correspondence.
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