Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3036009309

FEI Number

3036009309

Entity Name

BATENBURG APPLIED TECHNOLOGIES

City/State/Country

Rotterdam Zuid-Holland, NL

Establishment Address

Stolwijkstraat 33, Rotterdam Zuid-Holland 3079DN, NL

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Batenburg Applied Technologies (Owner Number: 10094133)

Owner / Operator Contact Address

Stolwijkstraat 33, Rotterdam, NL-ZH 3079DN, NL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Sirius Pintuition Base Unit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NEU	Marker, Radiographic, Implantable	General, Plastic Surgery	Class 2	878.4300	2025-11-17
PBY	Temporary Tissue Marker	General, Plastic Surgery	Class 2	878.4300	2025-11-17

Official Correspondent

Bram van Maurik

US Agent Details

Mindy McCann Email: usagent@qservegroup.com Phone: (424) 2718169

Related Public Records

Same Entity

Batenburg Applied Technologies

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3036009309. Last updated year: 2026. Please use registration number 3036009309 when referencing this establishment in official correspondence.