AB MEDICA GROUP S. A.

FDA Device Registration & Listing · Barcelona, ES · Registration 1000202462

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
1000202462
FEI Number
1000202462
Entity Name
AB MEDICA GROUP S. A.
City/State/Country
Barcelona, ES
Establishment Address
Calle Jerico 10 Bis Interior, Barcelona 08035, ES
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
AB Medica Group S. A. (Owner Number: 10092808)
Owner / Operator Contact Address
Calle Jerico 10 Bis Interior, Barcelona, ES-B 08035, ES
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AB Medica Group S.A

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DSF Recorder, Paper Chart Cardiovascular Class 1 870.2810 2025-02-20

Official Correspondent

Vanessa Sanchez Ramirez

US Agent Details

Adrian Mandreanu Email: adrian@amconsultingcorp.com Phone: (352) 2326658

Related Public Records

Same Entity

AB Medica Group S. A.
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
K770946 Instrumentation Laboratory CO RECORD, MODEL 702, I.L. 1977-07-05

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000202462. Last updated year: 2026. Please use registration number 1000202462 when referencing this establishment in official correspondence.
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