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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 2 of 13

Device	Model / Reference	Registries	Class	Status
Paq.90x90x20031sch.at4.mn.	2909002	FDA UDI	Class I	Active
Paq.210x300x1000/Eeg/100010	2421005	FDA UDI	Class I	Active
Paq.203x300x500 /eeg/140011gr	2420302	FDA UDI	Class I	Active
Paq.240x300x1000/Eeg/010001vh	2424001	FDA UDI	Class I	Active
Paq.60x75x250/ Oem St531/531i	2906005	FDA UDI	Class I	Active
Rollo 110x30x16i31bexen.mn.	1011011	FDA UDI	Class I	Active
Rollo 50x30x16i.fk-Nk-Bx(lm)	1005017	FDA UDI	Class I	Active
Paq.152x90x15031cor4305-Aao	2915200	FDA UDI	Class I	Active
Paq.240x300x1000/Eeg/000000.	2424002	FDA UDI	Class I	Active
Paq.345x300x1000/Eeg/000000	2434522	FDA UDI	Class I	Active
Paq.50x120x250.spacelabs	2905006	FDA UDI	Class I	Active
Rollo 75x25x12i.ph.heartstart	1007502	FDA UDI	Class I	Active
Paq.200x300x1000/Eeg/040001lp	2420008	FDA UDI	Class I	Active
Rollo 100x25x12e.printer.	0510001	FDA UDI	Class I	Active
Rollo 148x25x16e31siemen440	1014801	FDA UDI	Class I	Active
Paq.420x300x1000/Eeg/041000	2442007	FDA UDI	Class I	Active
Rollo 80x30x12e.heart Screen	1008011	FDA UDI	Class I	Active
Paq.176x300x1000/Qt-Ink/Eeg/	2417600	FDA UDI	Class I	Active
Paq.240x300x 500/Eeg/001000	2424003	FDA UDI	Class I	Active
Rollo 114x25x16i.printer	1011402	FDA UDI	Class I	Active
Paq.245x300x1000/Eeg/Nk Fv245-30	2424600	FDA UDI	Class I	Active
Paq.345x300x1000/Eeg/000020	2434523	FDA UDI	Class I	Active
Paq.345x300x1000/Eeg/001000.	2434502	FDA UDI	Class I	Active
Paq.50x70x26031k-312d.mn.	2905002	FDA UDI	Class I	Active
Rollo 110x50x16e31bg	1011007	FDA UDI	Class I	Active
Paq.210x300x250.mort.eli250	2921032	FDA UDI	Class I	Active
Rollo 110x30x12ihm(comindent)	1011013	FDA UDI	Class I	Active
Paq.410x300x1000/Eeg/100010.	2441002	FDA UDI	Class I	Active
Rollo 50x30x12e31printer.	1005008	FDA UDI	Class I	Active
Rollo 120x50x12i.siemens.	0512000	FDA UDI	Class I	Active
Paq.80x70x200/Qt-Hs80/Easote P8000	2908004	FDA UDI	Class I	Active
Paq.356x300x1000/Eeg/140011gr	2435600	FDA UDI	Class I	Active
Rollo 216x60x16e.nk(barasheed	1021608	FDA UDI	Class I	Active
Rollo 120x25x16e31printer.	1012003	FDA UDI	Class I	Active
Paq.110x100x20031bioset3700	2911002	FDA UDI	Class I	Active
Paq.215x280x200/Qt80brd007983	2921503	FDA UDI	Class I	Active
Paq.500x300x1000/Eeg/000000.	2450002	FDA UDI	Class I	Active
Rollo 144x30x16i.fk.nk.3c(lm)	1014408	FDA UDI	Class I	Active
Rollo 210x30x12e.printer	1021019	FDA UDI	Class I	Active
Rollo 57x15x12e.printer	1005718	FDA UDI	Class I	Active
Rollo 70x25x12e31printer	1007000	FDA UDI	Class I	Active
Rollo 210x30x16i.fk.(mes)	1021014	FDA UDI	Class I	Active
Paq.112x90x150.cadence	2911208	FDA UDI	Class I	Active
Paq.393x300x1000/Eeg/000000	2439300	FDA UDI	Class I	Active
Rollo 120x25x12e31printer	1012002	FDA UDI	Class I	Active
Rollo 78, 5x200x25e.printer	1007808	FDA UDI	Class I	Active
Rollo 57x25x12e.pri(barashed)	1005710	FDA UDI	Class I	Active
Rollo 63x30x16i/21/Fk-Nk.ts	1006301	FDA UDI	Class I	Active
Paq.348x300x 500/Eeg/100010	2434800	FDA UDI	Class I	Active
Paq.400x300x1000/Eeg/001000.	2440001	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