INFOMED SA

FDA Device Registration & Listing · Meinier Geneve, CH · Registration 3014272786

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
3014272786
FEI Number
3014272786
Entity Name
INFOMED SA
City/State/Country
Meinier Geneve, CH
Establishment Address
Route de compois 11, Meinier Geneve 1252, CH
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Infomed SA (Owner Number: 10056665)
Owner / Operator Contact Address
Route de Compois 11, Meinier, CH-GE 1252, CH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DIMI RRT Unit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System Gastroenterology, Urology Class 2 876.5860 2022-12-22

Official Correspondent

Oliver FAVRE

US Agent Details

George Hattub Business: Medicsense USA LLC Email: ghattub@comcast.net Phone: (508) 4796116

Related Public Records

Same Entity

Infomed SA
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K811830 Cordis Corp. C-DAK DUO-FLUX ARTIFICIAL KIDNEY 1981-09-21
K070320 Edwards Lifesciences Services GmbH EDWARDS AQUARIUS HEMOFILTRATION SYSTEM, MODEL ABM 01 2007-06-07
K150880 Outset Medical Tablo Console with Wireless Capability 2015-05-01

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0019-2025 Outset Medical, Inc. 2
Tablo Console, REF: PN-0003000, PN-0006000, part of the Tablo Hemodialysis System. The Tablo Hemodialysis System is indicated for use in patients with acute and/or chronic renal failure, with or without ultrafiltration, in an acute or chronic care facility.
Z-0028-2024 Fresenius Medical Care Holdings, Inc. 2
2008T Hemodialysis SYS, with CDX
Z-0029-2024 Fresenius Medical Care Holdings, Inc. 2
2008T Hemodialysis System without CDX
Z-0030-2024 Fresenius Medical Care Holdings, Inc. 2
2008T Hemodialysis System w/Bibag
Z-0031-2024 Fresenius Medical Care Holdings, Inc. 2
2008T GEN 2 Bibag without CDX

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3005695808 SARMED SRL IGLESIAS Sardegna, IT
3007137787 Nuwellis, Inc. Eden Prairie, MN, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014272786. Last updated year: 2026. Please use registration number 3014272786 when referencing this establishment in official correspondence.
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