ASCOM UMS SRL

FDA Device Registration & Listing · Scandicci Firenze, IT · Registration 3015173634

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
3015173634
FEI Number
3015173634
Entity Name
ASCOM UMS SRL
City/State/Country
Scandicci Firenze, IT
Establishment Address
Via Amilcare Ponchielli 29, Scandicci Firenze 50018, IT
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Ascom UMS srl (Owner Number: 10059298)
Owner / Operator Contact Address
Via Amilcare Ponchielli 29, Scandicci, IT-FI 50018, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Digistat Smart Central

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MSX System, Network And Communication, Physiological Monitors Cardiovascular Class 2 870.2300 2018-12-19

Official Correspondent

No official correspondent registered.

US Agent Details

Kevin Walls Business: Regulatory Insight, Inc. Email: kevin@reginsight.com Phone: (720) 9625412

Related Public Records

Same Entity

Ascom UMS srl
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
K973527 Data Critical Corp. CARDIO-PAGER SYSTEM 1998-03-31
K182637 Philips Medizin Systeme Boeblingen GmbH Philips IntelliVue XDS Software 2019-04-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015173634. Last updated year: 2026. Please use registration number 3015173634 when referencing this establishment in official correspondence.
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