Omnicell S.R.L.

FDA Device Registration & Listing · TRIESTE, IT · Registration 3006153342

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
3006153342
FEI Number
3006153342
Entity Name
Omnicell S.R.L.
City/State/Country
TRIESTE, IT
Establishment Address
Piazzale Legnami 1/b Edificio 9 Comprensorio Gaslini, TRIESTE 34145, IT
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Omnicell S.R.L. (HEALTH ROBOTICS) (Owner Number: 9090470)
Owner / Operator Contact Address
500 Cranberry Woods Drive, Cranberry Township, PA 16066, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

i.v.STATION i.v.STATION ONCO CYTOCARE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NEP System/Device, Pharmacy Compounding General Hospital Class 2 880.5440 2006-08-01

Official Correspondent

No official correspondent registered.

US Agent Details

Rachel Foster Business: OMNICELL Email: rachel.foster@omnicell.com Phone: (908) 4328742

Related Public Records

Same Entity

Omnicell S.R.L. (HEALTH ROBOTICS)
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006153342. Last updated year: 2026. Please use registration number 3006153342 when referencing this establishment in official correspondence.
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