Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009984513

FEI Number

3009984513

Entity Name

VASORUM

City/State/Country

Dublin, IE

Establishment Address

Trinitas House 2012, Orchard Avenue, Citywest Business Campus, Dublin D24, IE

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

Vasorum Ltd (Owner Number: 10052919)

Owner / Operator Contact Address

Trinitas House 2012, Orchard Avenue, Citywest Business Campus, Dublin, IE-D D24 WPW6, IE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P150006

All Registered Proprietary Names

Celt ACD Vascular Closure Device Celt ACD PLUS Vascular Closure Device

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MGB	Device, Hemostasis, Vascular	Unknown	Class 3	N/A	2016-10-18

Official Correspondent

James Coleman

US Agent Details

Matt Dryden Business: ProMedic Consulting LLC Email: matt.dryden@promedic.cc Phone: (239) 3076063

Related Public Records

Same Entity

Vasorum Ltd

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 3009984513. Last updated year: 2026. Please use registration number 3009984513 when referencing this establishment in official correspondence.