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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
—
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 9 of 13
DeviceModel / ReferenceRegistriesClassStatus
Rollo 144x30x16i.op(barashed) 1014409
FDA UDI
Class IActive
Paq.245x300x1000/Eeg/011020 2424511
FDA UDI
Class IActive
Rollo 50x45x16e. 1005040
FDA UDI
Class IActive
Paq.418x300x500 /eeg/000010 2441800
FDA UDI
Class IActive
Rollo 130x25x16e.k300(lm) 1013005
FDA UDI
Class IActive
Paq.345x300x1000/Eeg/011001vh 2434501
FDA UDI
Class IActive
Paq.200x300x 500/Eeg/001000 2420010
FDA UDI
Class IActive
Paq.345x300x 500/Eeg/101010 2434528
FDA UDI
Class IActive
Rollo 215x20x16i/Qt-Hs/Biolight E70/E80 1021504
FDA UDI
Class IActive
Rollo 112x30x16e*31*delta3+mn 1011203
FDA UDI
Class IActive
Paq.400x300x 500/Eeg/001000 2440010
FDA UDI
Class IActive
Paq.215x280x200/Qt80/Burd7868 3021501
FDA UDI
Class IActive
Paq.420x300x1000/Eeg/000000. 2442000
FDA UDI
Class IActive
Rollo 75x50x12e.printer 1007500
FDA UDI
Class IActive
Paq.153x300x1000/Eeg/000000 2415300
FDA UDI
Class IActive
Rollo 210x500x40, 5e.printer 1021017
FDA UDI
Class IActive
Rollo 50x45x16i.bd(saudi) 1005028
FDA UDI
Class IActive
Rollo 63x45x16i*31*printer. 1006302
FDA UDI
Class IActive
Rollo 216x50x25e*31*siemens. 1021602
FDA UDI
Class IActive
Rollo 110x20x12i/Qt-Hs/Bioset 3500 1011028
FDA UDI
Class IActive
Paq.215x300x1000/Eeg/100010 2421500
FDA UDI
Class IActive
Paq.486x300x1000/Qt-Ink/Eeg 2448600
FDA UDI
Class IActive
Paq.420x300x1000/Eeg/100000. 2442001
FDA UDI
Class IActive
ROLLO 80x60x25E/QT-HS/PRINTER 1008018
FDA UDI
Class IActive
PAQ. 210x140x200/QT-HS/FQW210-2-140 (C/ 2921071
FDA UDI
Class IActive
No Usar- Paq.100x150x120/Qt-Hs75/Ecg100 2910002
FDA UDI
Class IActive
Paq.245x300x1000/Eeg/001031dc 2424517
FDA UDI
Class IActive
Paq.243x300x1000/Eeg/001000 2424300
FDA UDI
Class IActive
Rollo 120x30x19e*31*k33/36.mn 1012001
FDA UDI
Class IActive
Rollo 63x45x12e.printer (hr) 1006309
FDA UDI
Class IActive
Rollo 90x20x19e*31*printer. 1009002
FDA UDI
Class IActive
Paq.112x90x300.suz-Kenz 2911202
FDA UDI
Class IActive
Rollo 50x20x16e*31*burd007958 1005021
FDA UDI
Class IActive
Rollo 120x30x19e.cr. 1012004
FDA UDI
Class IActive
Rollo 112x25x12e/Oem Btl Md 1011214
FDA UDI
Class IActive
Rollo 50x30x16e*31*printer 1005019
FDA UDI
Class IActive
Paq.106x140x200*31*burd7971mn 2910601
FDA UDI
Class IActive
Rollo 57x30x12e/Printer 1005716
FDA UDI
Class IActive
Paq.245x300x1000/Eeg/141021 2424520
FDA UDI
Class IActive
ROLLO 57x20x12E/QT-HS/COLSON CARDIPOCKE 1005727
FDA UDI
Class IActive
Rollo 80x300x25e/Qt-Ms120/Printer 1008013
FDA UDI
Class IActive
Rollo 63x30x16i.fk.(tecnom) 1006318
FDA UDI
Class IActive
Rollo 100x25x19e/Qt-80hs/Printer 1010000
FDA UDI
Class IActive
Rollo 57x25x12e*31*primedic. 1005705
FDA UDI
Class IActive
Rollo 125x30x16e/Qt-Hs/Pentam 1012500
FDA UDI
Class IActive
Paq.250x200x750*7b*ek36t.mn 2225000
FDA UDI
Class IActive
Rollo 45x30x16i.fk-Sa(gaesca) 1004501
FDA UDI
Class IActive
Paq.245x300x 500/Eeg/100010 2424519
FDA UDI
Class IActive
Rollo 57x6x8e.printer 1005721
FDA UDI
Class IActive
Paq.90x90x400*31*sch.at1.mn. 2909001
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