ARMSTRONG MEDICAL LTD.

FDA Device Registration & Listing · COLERAINE Northern Ireland, GB · Registration 9616692

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
9616692
FEI Number
3002226076
Entity Name
ARMSTRONG MEDICAL LTD.
City/State/Country
COLERAINE Northern Ireland, GB
Establishment Address
WATTSTOWN BUSINESS PARK, NEWBRIDGE RD., COLERAINE Northern Ireland BT52 1BS, GB
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ARMSTRONG MEDICAL LTD. (Owner Number: 9039632)
Owner / Operator Contact Address
WATTSTOWN BUSINESS PARK, NEWBRIDGE RD., COLERAINE, GB-CCG BT52 1BS, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AquaNase AMSORB Plus BUBBLE-BLOC BUBBLE-PLATE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAT Cannula, Nasal, Oxygen Anesthesiology Class 1 868.5340 2014-03-31
CBL Absorbent, Carbon-Dioxide Anesthesiology Class 1 868.5300 1999-11-16
BSF Absorber, Carbon-Dioxide Anesthesiology Class 1 868.5310 2011-05-10

Official Correspondent

No official correspondent registered.

US Agent Details

Kela Veshi Business: Kelaveshi Email: kelaveshi@yahoo.com Phone: (301) 7920964

Related Public Records

Same Entity

ARMSTRONG MEDICAL LTD.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0006-2008 Datex Ohmeda, Inc 1
GE Disposable Multi Absorber Canister used with EZchange Module for the Aisys, Avance, Aespire Anesthesia systems. The EZchange Module is an optional accessory for these anesthesia systems.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9616692. Last updated year: 2026. Please use registration number 9616692 when referencing this establishment in official correspondence.
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