COMPASS HEALTH BRANDS (DISTRIBUTION CENTER)

FDA Device Registration & Listing · Brook Park, OH, US · Registration 3005182235

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
3005182235
FEI Number
3005182235
Entity Name
COMPASS HEALTH BRANDS (DISTRIBUTION CENTER)
City/State/Country
Brook Park, OH, US
Establishment Address
18901 Snow Rd Bldg 6, Brook Park, OH 44142, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Compass Health Brands (Corporate Office) (Owner Number: 2182780)
Owner / Operator Contact Address
6753 Engle Rd, Middleburg Heights, OH 44130, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Meridian

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GAZ Tubing, Noninvasive General Hospital Class 2 880.6740 2017-02-06
BYX Tubing, Pressure And Accessories Anesthesiology Class 1 868.5860 2016-05-18
FNM Mattress, Air Flotation, Alternating Pressure General Hospital Class 2 880.5550 2016-05-18
FOX Stand, Infusion General Hospital Class 1 880.6990 2016-05-18

Official Correspondent

Elizabeth Proctor

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Compass Health Brands (Corporate Office)
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3012316249 COMPASS HEALTH BRANDS (CORPORATE OFFICE) Middleburg Heights, OH, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K910471 Baxter Healthcare Corp MEDID-VAC CLEAR NONCONDUCTIVE CONNECTING TUBE 1991-03-08

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005182235. Last updated year: 2026. Please use registration number 3005182235 when referencing this establishment in official correspondence.
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