ANETIC AID LTD

FDA Device Registration & Listing · Hampshire England, GB · Registration 3006975482

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
3006975482
FEI Number
3006975482
Entity Name
ANETIC AID LTD
City/State/Country
Hampshire England, GB
Establishment Address
44 New Lane, Havant, Hampshire England PO92NF, GB
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Anetic Aid Ltd (Owner Number: 10047262)
Owner / Operator Contact Address
44 New Lane, Havant, Hampshire, GB-NOTA PO9 2NF, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

QA4 Trolley System (Powered) AT4 Tourniquet System(Electronic) Single-use Sterile Tourniquet Cuff Six-use Day Tourniquet Cuff Reusable Tourniquet Cuff Rhys Davies Exsanguinator Padded Cuff Cover QA3 QA3 - Ophthalmic / Treatment

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GDC Table, Operating-Room, Electrical General, Plastic Surgery Class 1 878.4960 2014-07-29
KCY Tourniquet, Pneumatic General, Plastic Surgery Class 1 878.5910 2014-07-29
FPO Stretcher, Wheeled General Hospital Class 2 880.6910 2014-07-29
INK Stretcher, Wheeled, Powered Physical Medicine Class 2 890.3690 2025-11-20

Official Correspondent

Tim Schofield

US Agent Details

Steve Smargiasso Email: steve.smargiasso@aneticaid.com Phone: (817) 8465242

Related Public Records

Same Entity

Anetic Aid 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-0023-05 Stryker Medical 2
Stryker brand Rugged EZ-Pro R4 Ambulance Cot, model 6092.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006975482. Last updated year: 2026. Please use registration number 3006975482 when referencing this establishment in official correspondence.
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