Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004627792

FEI Number

1000654629

Entity Name

Pfizer Manufacturing Belgium NV

City/State/Country

Puurs-Sint-Amands Antwerpen, BE

Establishment Address

Rijksweg 12, Puurs-Sint-Amands Antwerpen 2870, BE

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

PFIZER INC. (Owner Number: 9924008)

Owner / Operator Contact Address

275 N Field Drive, Lake Forest, IL 60045, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Genotropin Pen

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NSC	Injector, Pen	General Hospital	Class 2	880.5860	2016-05-11

Official Correspondent

Kathleen Lins

US Agent Details

Kathleen Lins Business: PFIZER INC. Email: rscmoppgp-druglisting@pfizer.com Phone: (224) 2124842

Related Public Records

Same Entity

PFIZER INC.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3004945409	Pfizer Inc	Parsippany, NJ, US
3002522469	Pfizer Service Company BV	Zaventem Vlaams Brabant, BE
1925262	HOSPIRA, INC.	MCPHERSON, KS, US
1810189	PHARMACIA & UPJOHN COMPANY LLC	KALAMAZOO, MI, US
1000150646	Wyeth Pharmaceuticals LLC	Collegeville, PA, US

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9681538	SCANDINAVIAN HEALTH LTD.	Taoyuan City, TW
2182861	ANTARES PHARMA, INC.	Minnetonka, MN, US
3012775596	SHALON CHEMICAL INDUSTRIES LTD.	Kiryat Gat Southern, IL

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004627792. Last updated year: 2026. Please use registration number 3004627792 when referencing this establishment in official correspondence.