Moog Costa Rica, SRL

FDA Device Registration & Listing · Alajuela San Jose, CR · Registration 3008058400

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
3008058400
FEI Number
3008058400
Entity Name
Moog Costa Rica, SRL
City/State/Country
Alajuela San Jose, CR
Establishment Address
Coyol Free Zone and Business Park, Alajuela San Jose 20113, CR
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
MOOG, INC. (Owner Number: 9086921)
Owner / Operator Contact Address
4314 Zevex Park Lane, Salt Lake City, UT 84123, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Pump, Infusion ENFit Enteral Administration Sets

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FRN Pump, Infusion General Hospital Class 2 880.5725 1999-08-06
PIF Gastrointestinal Tubes With Enteral Specific Connectors Gastroenterology, Urology Class 2 876.5980 2015-04-16

Official Correspondent

Christopher Dodge

US Agent Details

Chris Dodge Business: MOOG, INC. Email: mmdg-ra@moog.com Phone: (801) 2641001

Related Public Records

Same Entity

MOOG, 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
1722139 ZEVEX, INC. Salt Lake City, UT, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K913718 Abbott Laboratories PANCRETEC I.V. MODEL 5000 INFUS DEVICE, MODIFIED 1991-10-30
K840616 Advanced Bio Systems, Inc. MINI-PUMP U-100 1984-03-30
K850183 Deltec Systems, Inc. CADD-VT, 5300 AMBULATORY INFUSION PUMP W/3050, 50M 1985-03-13

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0001-2011 Baxter Healthcare Corp. Rt. 2
Baxter Colleague Single Channel Volumetric Infusion Pumps. Baxter Healthcare Corporation, Medication Delivery Division. Product Codes: 2M8151, 2M8161, and 2M9161.
Z-0002-2011 Baxter Healthcare Corp. Rt. 2
Baxter Colleague Triple Channel Volumetric Infusion Pumps. Baxter Healthcare Corporation, Medication Delivery Division. Product codes: 2M8153, and 2M8163.
Z-0005-2025 Zyno Medical LLC 2
Z-800 Infusion System, Model Numbers Z-800, Z-800F, Z-800W, Z-800WF; Software Version: Z-800 6.1.01 and 6-1.07z; Z-800F 4.1.02 and 4.1.08z; Z-800W 3.1.32 and 3.1.64z, Z-800WF 3.1.32 and 3.1.64z
Z-0006-2011 CareFusion Corporation 2
CareFusion Alaris PC Unit Model 8015 (formerly Medley PC Unit): Alaris PC Units (Model 8015) with logic board part number TC10005522 manufactured and serviced between December 20, 2008 and May 6, 2009; and Alaris PC Units (with logic board part number TC10005572 manufactured and serviced between May 7, 2009 and September 8, 2009. For use with Alaris infusion and monitoring systems.
Z-0007-2012 B Braun Medical, Inc 2
Outlook ES Safety Infusion System, Model 621-100ES, 621-200ES, 621-300ES, and 621-400ES B. Braun Medical Inc., 1601 Wallace Drive, Suite 150, Carrollton, TX 75006 The Outlook ES pump is intended for use with B. Braun Medical Inc., Horizon Pump IV Sets to regulate the flow of primary and secondary fluids when positive pressure is required.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008058400. Last updated year: 2026. Please use registration number 3008058400 when referencing this establishment in official correspondence.
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