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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 5 of 13
DeviceModel / ReferenceRegistriesClassStatus
Rollo 75x25x12i/Printer 1007503
FDA UDI
Class IActive
Paq.112x100x200/Goldway Ut3000 2911209
FDA UDI
Class IActive
Rollo 45x30x16i.fukuda-Sa-Hp 1004500
FDA UDI
Class IActive
Rollo 50x30x16i.hp-40451/3/7a 1005000
FDA UDI
Class IActive
PAQ. 112x100x300 ELAN 1100 - OEM ET MED 2911211
FDA UDI
Class IActive
Paq.345x300x1000/Eeg/131000 2434509
FDA UDI
Class IActive
Paq.215x280x200/Qt-Hs80/Q-4500 2921511
FDA UDI
Class IActive
Rollo 50*30*16i.hp(saudi) 1005029
FDA UDI
Class IActive
Rollo 80x75x25e.printer. 1008009
FDA UDI
Class IActive
Paq.300x300x1000/Eeg/001000 2430000
FDA UDI
Class IActive
Rollo 110x30x16i.ergocid Card 1011017
FDA UDI
Class IActive
Rollo 58x25x12e*31*b5eco 1005802
FDA UDI
Class IActive
Rollo 110x30x12i*31*hormann. 1011003
FDA UDI
Class IActive
Paq.215x280x250.mortara Tmx425 2921519
FDA UDI
Class IActive
Rollo 50x30x16i.op-12ke(tecn) 1005033
FDA UDI
Class IActive
Rollo 106x80x40, 5i/Qt-Hs/Printer 1010606
FDA UDI
Class IActive
Rollo 216x45x16e*31*nk.3c.mn. 1021600
FDA UDI
Class IActive
Rollo 114x45x12e*31*printer. 1011401
FDA UDI
Class IActive
Paq.63x100x400*31*fk.501ax.mn 2906301
FDA UDI
Class IActive
Paq.180x300x 500/Eeg/140011gr 2418001
FDA UDI
Class IActive
Rollo 63x30x16i.fk(letoile) 1006319
FDA UDI
Class IActive
Rollo 55x30x16e/Qt-Hs/Red Grid 1005505
FDA UDI
Class IActive
Rollo 50x30x16i*31*fk-Black 1005018
FDA UDI
Class IActive
Rollo 108x23x16e*31*mortara. 1010801
FDA UDI
Class IActive
Rollo 63x30x16i.fk.black 1006316
FDA UDI
Class IActive
Paq.400x300x1000/Eeg/000000 2440014
FDA UDI
Class IActive
Rollo 50x30x16i.op-12ke(hr) 1005026
FDA UDI
Class IActive
Paq.390x300x1000/Eeg/040001lp 2439007
FDA UDI
Class IActive
ROLLO 78, 5x10x8I/QT-HS/RED GRID x BEXEN 1007802
FDA UDI
Class IActive
Paq.343x300x500 /eeg/141011gr 2434307
FDA UDI
Class IActive
Rollo 183x30x19e*31*cr-Kenz. 1018300
FDA UDI
Class IActive
ROLLO 152x20x12I/QT-HS/BIONET FC1400 1015201
FDA UDI
Class IActive
Paq.447x300x1000/Eeg/001010 2444700
FDA UDI
Class IActive
Paq.455x300x1000/Eeg/000020 2445502
FDA UDI
Class IActive
Rollo 106x25x16i/Qt-Hs/Reanibex 800 1010607
FDA UDI
Class IActive
Paq.210x280x200.wa Cp100/200 2921035
FDA UDI
Class IActive
Rollo 50x45x16i.burd.ek10(lm) 1005024
FDA UDI
Class IActive
Paq.80x70x315/Qt-Hs55/Sch.at101 2908006
FDA UDI
Class IActive
Rollo 90x50x19e*31*remeda. 1009000
FDA UDI
Class IActive
Rollo 112x25x12e/Qt-Hs/Mir Oem 910350 1011220
FDA UDI
Class IActive
Paq.390x300x1000/Eeg/001000. 2439002
FDA UDI
Class IActive
Rollo 57x11x8e/Webeco-41602.4 1005720
FDA UDI
Class IActive
Rollo 110x180x12e/Qt-Hs/Printer 1011027
FDA UDI
Class IActive
Rollo 126x25x12e.printer 1012600
FDA UDI
Class IActive
Paq.345x300x1000/Eeg/221000. 2434506
FDA UDI
Class IActive
Rollo 120x30x12e.printer 1012011
FDA UDI
Class IActive
Rollo 120x20x19e/Ar1200 1012009
FDA UDI
Class IActive
Rollo 57x10x12e*31*printer. 1005704
FDA UDI
Class IActive
Paq.245x300x1000/Eeg/011021vh 2424508
FDA UDI
Class IActive
Rollo 60x45x12e*31*printer. 1006003
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