Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030927791

FEI Number

3030927791

Entity Name

ACIME FRAME

City/State/Country

Rinxent Pas-de-Calais, FR

Establishment Address

1 avenue de l'Europe, Z.A. de la Maie, Rinxent Pas-de-Calais 62720, FR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Acime Frame (Owner Number: 10090568)

Owner / Operator Contact Address

1 avenue de l'Europe, Z.A. de la Maie, Rinxent, FR-62 62720, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SKOT SILVER (Stretcher) SKOT (Stretcher) Manchester Lourde Charge (Transfer Chair) Manchester INN (Transfer Chair) Manchester 3 (Transfer Chair)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FPO	Stretcher, Wheeled	General Hospital	Class 2	880.6910	2024-04-13
FMR	Device, Transfer, Patient, Manual	General Hospital	Class 1	880.6785	2024-04-13

Official Correspondent

No official correspondent registered.

US Agent Details

Stephan Toupin Business: Dawa Medical LLC Email: stoupin@dawamedical.com Phone: (786) 7311159

Related Public Records

Same Entity

Acime Frame

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 3030927791. Last updated year: 2026. Please use registration number 3030927791 when referencing this establishment in official correspondence.