DUPHAMED B.V.

FDA Device Registration & Listing · ALPHEN AAN DEN RIJN Zuid-Holland, NL · Registration 3005739556

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
3005739556
FEI Number
3005739556
Entity Name
DUPHAMED B.V.
City/State/Country
ALPHEN AAN DEN RIJN Zuid-Holland, NL
Establishment Address
Jac.P.Thijsseweg 12, ALPHEN AAN DEN RIJN Zuid-Holland 2408 ER, NL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
DUPHAMED B.V. (Owner Number: 9087279)
Owner / Operator Contact Address
Jac.P.Thijsseweg 12, --, ALPHEN AAN DEN RIJN, NL-NOTA 2408 ER, NL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

dental x-ray sensor holder

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EHB Collimator, X-Ray Dental Class 1 872.1840 2006-05-17

Official Correspondent

No official correspondent registered.

US Agent Details

Alan Schwartz Business: MDI Consultants, Inc. Email: alan@mdiconsultants.com Phone: (516) 4829001

Related Public Records

Same Entity

DUPHAMED B.V.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K781675 General X-Ray, Inc. X-RAY COLLIMATOR 1978-12-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005739556. Last updated year: 2026. Please use registration number 3005739556 when referencing this establishment in official correspondence.
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