Merrimack Manufacturing

FDA Device Registration & Listing · Manchester, NH, US · Registration 3044561902

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
3044561902
FEI Number
3044561902
Entity Name
Merrimack Manufacturing
City/State/Country
Manchester, NH, US
Establishment Address
350 Gay St, Manchester, NH 03103, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Merrimack Manufacturing (Owner Number: 10062587)
Owner / Operator Contact Address
540 North Commercial Ave, STE 110, Manchester, NH 03101, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

twiist Automated Insulin Delivery (AID) System Powered by Tidepool; Twiist AID System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NDC Calculator, Drug Dose Anesthesiology Class 2 868.1890 2025-02-21
QFG Alternate Controller Enabled Insulin Infusion Pump Clinical Chemistry Class 2 880.5730 2025-02-21

Official Correspondent

Priya Sampath

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Merrimack Manufacturing
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3015192982 MERRIMACK MANUFACTURING Manchester, NH, US

Similar Registrations

Registration Number Establishment Name Location
3006400278 Picis Clinical Solutions, S.A.U. BARCELONA, ES
3010817588 MEDICAL DECISION NETWORK Charlottesville, VA, US
3017986070 BIOINTELLISENSE INC. Golden, CO, US
3025343017 COMERGE AG Zurich, CH
2032227 MEDTRONIC MINIMED NORTHRIDGE, CA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3044561902. Last updated year: 2026. Please use registration number 3044561902 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.