Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9610348

FEI Number

3002806617

Entity Name

Curium Netherlands B.V.

City/State/Country

Petten Noord-Holland, NL

Establishment Address

Westerduinweg 3, 1755 LE, Petten Noord-Holland 1755 ZG, NL

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Curium US LLC (Owner Number: 10051585)

Owner / Operator Contact Address

2703 Wagner Place, Maryland Heights, MO 63043, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

IR-192 Source IR-192

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JAQ	System, Applicator, Radionuclide, Remote-Controlled	Radiology	Class 2	892.5700	2016-04-07
JAQ	System, Applicator, Radionuclide, Remote-Controlled	Radiology	Class 2	892.5700	2016-04-07

Official Correspondent

No official correspondent registered.

US Agent Details

Bridget Martin Business: Curium US LLC Email: Bridget.Martin@curiumpharma.com Phone: (314) 3437518

Related Public Records

Same Entity

Curium US LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3011353845	Curium US LLC	Maryland Heights, MO, US

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9611894	NUCLETRON B.V.	VEENENDAAL Utrecht, NL
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9610348. Last updated year: 2026. Please use registration number 9610348 when referencing this establishment in official correspondence.