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Maco Pharma

Active in EUDAMED

Francefrom SRN EUDAMED FDA SRN FR-MF-000001657 FEI 3004404323

Maco Pharma is a medical device manufacturer based in France, with 273 devices listed in EUDAMED and FDA GUDID (EU Class IIb, III, IIa and I) as of 14 Nov 2026.

Devices
273
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 14 Nov 2026

Registries
  • EUDAMED 258
  • FDA GUDID 17

A device listed in two registries counts in both.

Device classes
  • EU Class IIb 196
  • EU Class III 29
  • EU Class IIa 19
  • EU Class I 14
  • FDA Class II 9
  • FDA Class I 6
Identifiers
  • EUDAMED SRN FR-MF-000001657
  • FDA FEI 3004404323
  • DUNS 577149081

At a glance

Counted by deviCERTS from registry records

EU certificates

4 of 4 in force.

See certificates

Market reach

European Union
EUDAMED actor, 4 certificates
United States
FDA FEI

Catalogue273

Newest first, rows 1-50 of 273

Search and filter all 273 devices
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Rows 1-50 of 273

Showing 1-50 of 273

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
FR-MF-000001657
FDA FEI number
3004404323
DUNS number
577149081
EU VAT number
FR31391600905
EUDAMED status
Active
EUDAMED registered name
MACO PHARMA
Registered address
Lorthiois, 59420, MOUVAUX, France
Phone
770-270-6867
PRRC contact
Raouf BENYAMINA(public in EUDAMED)

EUDAMED certificates4

4 certificates4 valid, 0 expiredMDR 4next expiry 16 Jan 2029

EUDAMED certificates (4)

GMED SAS 0459 4 certificates

  • 40558 Active Amended

    Quality management system EU MDR

    Issued
    8 Oct 2026
    Expires
    24 Jun 2031
    Reason
    Other
  • 40346 Active Supplemented

    Quality management system EU MDR

    Issued
    8 Oct 2026
    Expires
    20 Oct 2030
    Reason
    Other
  • 39531 Active Supplemented

    Quality management system EU MDR

    Issued
    8 Oct 2026
    Expires
    16 Jan 2029
    Reason
    Other
  • 39532 Active Amended

    Technical documentation EU MDR

    Issued
    8 Oct 2026
    Expires
    16 Jan 2029
    Reason
    Other

Frequently asked questions

How many devices does MACO PHARMA have in the registry?

The registry currently lists 273 devices for MACO PHARMA. Devices recorded under merged duplicate company entries are counted once.

Which registries list MACO PHARMA's devices?

Among its 50 most recently registered devices, MACO PHARMA has devices listed in EUDAMED (50 devices).

What risk classes do MACO PHARMA's devices fall under?

Among its 50 most recently registered devices, the classes recorded for MACO PHARMA's devices are Class I, Class IIa, Class IIb and Class III. Each device page shows its own class and authorisation.

What EUDAMED certificates are recorded for MACO PHARMA?

EUDAMED lists 4 certificates for MACO PHARMA (quality management system; technical documentation) under MDR. The most recent was issued on 8 Oct 2026.

What are the newest devices from MACO PHARMA in the registry?

The most recently registered devices listed for MACO PHARMA include Single or multiple blood bags with LCRD2 filter, Red Cell Additive Solution SAG-Mannitol, Single or multiple blood bags with Plas4 filter and THERAFLEX MB-Plasma.

Generated automatically from registry data and not verified by a human reviewer.