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AB MEDICA GROUP, S.A.

US

Last updated May 23, 2026

What AB MEDICA GROUP, S.A. makes

AB Medica Group produces electrocardiographic (ECG) recording paper and associated printer rolls, including standard and specialty formats for medical diagnostic equipment. Their products include rolls for ECG printers, EEG systems, and other diagnostic devices, designed to record and print physiological data.

The company’s portfolio consists of Class I medical devices, which are generally considered low-risk. These products are listed in the FDA’s Unique Device Identification (UDI) database, ensuring traceability and regulatory compliance in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does AB Medica Group, S.A. manufacture?

AB Medica Group, S.A. specializes in producing electrocardiographic (ECG) recording paper and associated printer rolls. These include standard and specialty formats designed for ECG printers, EEG systems, and other diagnostic devices that record and print physiological data. Their products are primarily consumables used in medical diagnostics.

Where is AB Medica Group, S.A. based?

AB Medica Group, S.A. is based in the United States. The company’s focus is on manufacturing medical consumables, particularly for diagnostic equipment used in healthcare settings.

Which regulatory registries list AB Medica Group’s devices?

AB Medica Group’s devices are listed in the FDA’s Unique Device Identification (UDI) database. This registry ensures traceability and compliance for Class I medical devices, which are generally considered low-risk. Listing in the UDI database helps facilitate regulatory oversight and transparency in the U.S. market.

How are AB Medica Group’s devices classified under medical device regulations?

AB Medica Group’s devices fall under Class I classification, which is the lowest risk category for medical devices. This classification is typically assigned to products like consumables (e.g., ECG recording paper) that pose minimal risk to patients and users. Class I devices are generally exempt from strict pre-market approval but still require compliance with good manufacturing practices and other regulatory requirements.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
460037021

Catalogue (621)

Page 3 of 13
DeviceModel / ReferenceRegistriesClassStatus
Paq.270x300x1000/Eeg/Ink-Hq 2427000
FDA UDI
Class IActive
Rollo 75x40x12.printer 0507500
FDA UDI
Class IActive
Paq.50x100x300*31*n.kohden. 2905003
FDA UDI
Class IActive
Paq.245x300x1000/Eeg/101010. 2424502
FDA UDI
Class IActive
Paq.240x300x500/Eeg/000000 2424005
FDA UDI
Class IActive
Paq.63x100x200.fk501.mn 2906306
FDA UDI
Class IActive
Paq.345x300x 500/Eeg/001000 2434527
FDA UDI
Class IActive
Rollo 110x15x12e*31*printer. 1011005
FDA UDI
Class IActive
Rollo 60x30x16e/Delt.1plus(lm 1006016
FDA UDI
Class IActive
ROLLO 63x25x16I/QT-HS/FK-NK 1006323
FDA UDI
Class IActive
Paq.111x100x150 Sunray/Comen (fhr240) 2911103
FDA UDI
Class IActive
Paq.245x300x1000/Eeg/001001ds 2424503
FDA UDI
Class IActive
Rollo 112x30x12e*31*heartscre 1011209
FDA UDI
Class IActive
Rollo 63x45x12e*31*printer. 1006304
FDA UDI
Class IActive
Rollo 50x30x16i.fk-Nk(2mm) 1005030
FDA UDI
Class IActive
Paq.110x100x300*31*nk.bl.mn. 2911000
FDA UDI
Class IActive
PAQ. 60x75x266 AR600-OEM ET MEDICAL 2906007
FDA UDI
Class IActive
Rollo 110x30x16i*31*bexen.mn. 1011012
FDA UDI
Class IActive
Rollo 60x30x16e/Delt1(etoile) 1006019
FDA UDI
Class IActive
Rollo 110x10x8e.printer. 1011019
FDA UDI
Class IActive
Rollo 76, 5x40x12e.printer. 0507600
FDA UDI
Class IActive
Rollo 80x20x12e/Qt-Hs/Mindray-Edan 1008017
FDA UDI
Class IActive
Paq.110x140x100.fukuda Fx7202 2911006
FDA UDI
Class IActive
Rollo 58x25x12e/Oem Btl08s 1005806
FDA UDI
Class IActive
Rollo 37x25x12e*31*printer.ts 1003701
FDA UDI
Class IActive
Rollo 50x30x19e*31*ote.c1 1005001
FDA UDI
Class IActive
Rollo 50x50x16i.hellige Ek31 1005046
FDA UDI
Class IActive
PAQ. 60x100x300 DELTA 1+ - OEM ET MEDIC 2906006
FDA UDI
Class IActive
Rollo 50x30x16i.fk-Nk(gaesca) 1005023
FDA UDI
Class IActive
Paq.345x300x1000/Eeg/101010. 2434503
FDA UDI
Class IActive
Rollo 90x28x19e*31*p-80. 1009001
FDA UDI
Class IActive
Rollo 144x30x16i*31*fk-Nk.3c. 1014405
FDA UDI
Class IActive
Rollo 112x25x12e*31*printer. 1011200
FDA UDI
Class IActive
Paq.245x300x1000/Eeg/041031lp 2424515
FDA UDI
Class IActive
Paq.108x140x200.eli-150 2910800
FDA UDI
Class IActive
Paq.360x300x1000/Eeg/001000. 2435604
FDA UDI
Class IActive
Rollo 110x25x16e/Qt-Hs/Red Grid 1011015
FDA UDI
Class IActive
Paq.245x300x0500/Eeg/141020 2424521
FDA UDI
Class IActive
Rollo 50x20x16i.printer 1005047
FDA UDI
Class IActive
ROLLO 112x25x12E/OEM BTL MD/PHENOL FREE 1011224
FDA UDI
Class IActive
Paq.90x70x400*31*ote.p-80. 2909000
FDA UDI
Class IActive
Rollo 80x102x12e/Qt-Hs/Sescam-Sitas 1008016
FDA UDI
Class IActive
Paq.155x300x1000/Eeg/101011tm 2415501
FDA UDI
Class IActive
Paq.110x140x150.ge.mac800 2911010
FDA UDI
Class IActive
Paq.400x300x1000/Eeg/011021vh 2440006
FDA UDI
Class IActive
Rollo 57x50x12e.printer 1005713
FDA UDI
Class IActive
Paq.210x280x250.mort.eli380 2921089
FDA UDI
Class IActive
Paq.200x300x1000/Eeg/ 2420009
FDA UDI
Class IActive
Rollo 112x25x12e*31*b56/A4 1011205
FDA UDI
Class IActive
Rollo 210x20x16e.ascard 612 1021013
FDA UDI
Class IActive

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Ab Medica Group S. A. Barcelona · ES FEI 1000202462