Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005042488

FEI Number

3005042488

Entity Name

West Contract Manufacturing, LLC

City/State/Country

Cidra, PR, US

Establishment Address

State Rd. #1 Km. 48.7, BO. BEATRIZ, Cidra, PR 00739, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

WEST PHARMACEUTICAL SERVICES, INC. (Owner Number: 2514921)

Owner / Operator Contact Address

530 Herman O. West Drive, Exton, PA 19341, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Vial2Bag 20mm Admixture Device

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LHI	Set, I.V. Fluid Transfer	General Hospital	Class 2	880.5440	2020-10-28

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

WEST PHARMACEUTICAL SERVICES, 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
3015176617	West Pharmaceutical Services AZ, Inc.	Scottsdale, AZ, US
3010893867	Tech Group Europe Limited t/a West	Mulhaddart Dublin, IE
2032861	West Pharmaceutical Services Arizona, Inc.	Tempe, AZ, US
2032862	West Pharmaceutical Services AZ, Inc.	SCOTTSDALE, AZ, US
3000223297	West Pharma. Services IL, Ltd.	Ra'anana Central, IL

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K243985	Icu Medical, Inc.	Rio Drug Reconstitution Transfer Device	2025-01-22
K222718	Hangzhou Qiantang Longyue Biotechnology Co., Ltd.	Vial Adapter	2023-03-10

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0007-2017	Baxter Corporation Englewood	2	0.2 Micron Filter, 50 mm Product Usage: The 0.2 Micron Filter is a bacteria and particulate filter for aqueous solutions. It attaches to a standard Baxter Pharmacy Pump Tube Set.

Similar Registrations

Registration Number	Establishment Name	Location
3043226252	ZAPALIGN LLC	Fort Lauderdale, FL, US
2523676	B. BRAUN US DEVICE MANUFACTURING LLC	ALLENTOWN, PA, US
3016418550	Takeda Pharmaceuticals U.S.A., Inc.	Cambridge, MA, US
3042177665	PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.	BEST Noord-Brabant, NL
3012798826	BD SWITZERLAND SARL	Eysins Vaud, CH

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005042488. Last updated year: 2026. Please use registration number 3005042488 when referencing this establishment in official correspondence.