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AB MEDICA GROUP, S.A.

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: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 460037021

Catalogue (621)

Page 1 of 13

Device	Model / Reference	Registries	Class	Status
Rollo 50x45x16i.bd(comindent)	1005036	FDA UDI	Class I	Active
Paq.345x300x1000/Eeg/001050	2434517	FDA UDI	Class I	Active
Rollo 209x20x205ek600(etoile	1020901	FDA UDI	Class I	Active
Rollo 57x12x12e.ts.	1005709	FDA UDI	Class I	Active
Rollo 50x30x16i.black	1005043	FDA UDI	Class I	Active
Rollo 58x25x12e.print.(2mm)	1005804	FDA UDI	Class I	Active
Rollo 50x30x16i.fk.nk.(lm)	1005034	FDA UDI	Class I	Active
Paq.345x300x500 /eeg/011000	2434526	FDA UDI	Class I	Active
Rollo 120x60x12e.printer	1012012	FDA UDI	Class I	Active
Paq.170x150x500n3ek403t.mn.	2217001	FDA UDI	Class I	Active
Rollo 278x30x16i.nk.	1027800	FDA UDI	Class I	Active
Rollo 50x30x16e.black	1005044	FDA UDI	Class I	Active
Paq.112x100x30031delta3.mn.	2911200	FDA UDI	Class I	Active
Rollo 108x23x19e31marquette	1010800	FDA UDI	Class I	Active
Paq.390x300x500/Ink-Hq	2439010	FDA UDI	Class I	Active
Paq.60x100x300.cr.delta 1plus	2906003	FDA UDI	Class I	Active
Rollo 109x25x12e31printer.	1010900	FDA UDI	Class I	Active
ROLLO 56x25x19I/QT-HS/RED GRID	1005600	FDA UDI	Class I	Active
Rollo 60x15x15e.st Oem 531/531i	1006024	FDA UDI	Class I	Active
Paq.125x300x1000/Eng/300010.	2412501	FDA UDI	Class I	Active
Paq.346x300x1000/Eeg/001000	2434600	FDA UDI	Class I	Active
Rollo 110x20x12e/Qt-Hs/Zondan	1011026	FDA UDI	Class I	Active
Paq.215x280x30028case-12.1p	3021500	FDA UDI	Class I	Active
Paq.216x300x1000/Eeg/140011gr	2421600	FDA UDI	Class I	Active
Rollo 215x25x16e.cardiocare	1021503	FDA UDI	Class I	Active
Rollo 210x30x16i.op(barashed)	1021008	FDA UDI	Class I	Active
Rollo 50x30x16e31kramer	1005020	FDA UDI	Class I	Active
Paq.398x300x500/Eeg/100010	2439804	FDA UDI	Class I	Active
Paq.343x300x1000/Eeg	2434301	FDA UDI	Class I	Active
Paq.230x300x1000/Eeg/140011gr	2423003	FDA UDI	Class I	Active
Paq.398x300x1000/Eeg/100010.	2439800	FDA UDI	Class I	Active
Paq.112x90x160.cadence	2911205	FDA UDI	Class I	Active
Paq.420x300x1000/Eeg/000030	2442004	FDA UDI	Class I	Active
ROLLO 210x30x19E DELTA 60 - OEM ET MEDI	1021021	FDA UDI	Class I	Active
ROLLO 216x50x19E/QT-HS/SIEMENS	1021609	FDA UDI	Class I	Active
Rollo 60x50x16i/Gr55/Im.si.	1006005	FDA UDI	Class I	Active
Paq.343x300x1000/Eeg/001000.	2434300	FDA UDI	Class I	Active
Paq.215x280x250.mort.eli250	2921507	FDA UDI	Class I	Active
Rollo 60x20x12e31printer.	1006007	FDA UDI	Class I	Active
Rollo 57x75x12e31printer	1005707	FDA UDI	Class I	Active
Paq.334x300x1000/Eeg/100010	2433400	FDA UDI	Class I	Active
Rollo 60x23x12i31bg	1006009	FDA UDI	Class I	Active
Rollo 50x20x12i.mindray	1005045	FDA UDI	Class I	Active
Rollo 80x160x25e31printer	1008008	FDA UDI	Class I	Active
Rollo 250x50x19e31remeda.	1025000	FDA UDI	Class I	Active
Paq.245x300x500 /eeg/141021ad	2424514	FDA UDI	Class I	Active
Rollo 110x25x12e.pr(barashed)	1011010	FDA UDI	Class I	Active
Paq.330x300x1000/Eeg/100010	2433001	FDA UDI	Class I	Active
Rollo 106x110x16e.printer.	1010603	FDA UDI	Class I	Active
Paq.100x150x180/Qt-Hs75/Cardioline Ecg1	2910000	FDA UDI	Class I	Active

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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