Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008958625

FEI Number

3008958625

Entity Name

APOTHICOM DISTRIBUTION

City/State/Country

Paris Ile-de-France, FR

Establishment Address

52 Avenue Edison, Paris Ile-de-France 75013, FR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Apothicom Distribution (Owner Number: 10035727)

Owner / Operator Contact Address

52 Avenue Edison, Paris, FR-IDF 75013, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

STERIFILT BASIC STERIFILT FAST STERIFILT PLUS DISPENSER, LIQUID MEDICATION

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JRL	Unit, Filter, Membrane	Clinical Chemistry	Class 1	862.2050	2011-03-18
KYX	Dispenser, Liquid Medication	General Hospital	Class 1	880.6430	2011-03-18

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Apothicom Distribution

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
K812750	Instrumentation Laboratory CO	IL 703, STAT SEPARATOR	1982-01-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008958625. Last updated year: 2026. Please use registration number 3008958625 when referencing this establishment in official correspondence.