ECLS

FDA Device Registration & Listing · Saint Louis, MO, US · Registration 3043040746

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
3043040746
FEI Number
3043040746
Entity Name
ECLS
City/State/Country
Saint Louis, MO, US
Establishment Address
190 Carondelet Plz Ste 1450, Saint Louis, MO 63105, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
ECLS (Owner Number: 10095020)
Owner / Operator Contact Address
190 Carondelet Plaza, Suite 1450, Saint Louis, MO 63105, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ProCart Protego

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EAK Screen, Leaded, Operator Radiation Protector Radiology Class 1 892.6500 2026-01-15

Official Correspondent

David Mills

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ECLS
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043040746. Last updated year: 2026. Please use registration number 3043040746 when referencing this establishment in official correspondence.
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