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AMO Uppsala AB

Sweden SE-MF-000017467 Last updated 23 Oct 2026

Devices
46
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue46

  • 10272015 Ref 10272015

    Class IIb EUDAMED Active

  • 10271016 Ref 10271016

    Class III EUDAMED Active

  • 10332014 Ref 10332014

    Class IIb EUDAMED Active

  • 10290015 Ref 10290015

    Class IIb EUDAMED Active

  • 10291012 Ref 10291012

    Class IIb EUDAMED Active

  • 10312015 Ref 10312015

    Class IIb EUDAMED Active

  • 10270015 Ref 10270015

    Class IIb EUDAMED Active

  • 10311012 Ref 10311012

    Class IIb EUDAMED Active

  • 10270012 Ref 10270012

    Class IIb EUDAMED Active

  • 10271015 Ref 10271015

    Class IIb EUDAMED Active

  • 10310014 Ref 10310014

    Class IIb EUDAMED Active

  • 10312012 Ref 10312012

    Class IIb EUDAMED Active

  • 10290012 Ref 10290012

    Class IIb EUDAMED Active

  • 10310015 Ref 10310015

    Class IIb EUDAMED Active

  • 10282014 Ref 10282014

    Class IIb EUDAMED Active

  • 10312014 Ref 10312014

    Class IIb EUDAMED Active

  • 10270011 Ref 10270011

    Class IIb EUDAMED Active

  • 10272514 Ref 10272514

    Class IIb EUDAMED Active

  • 10270514 Ref 10270514

    Class IIb EUDAMED Active

  • 10270014 Ref 10270014

    Class IIb EUDAMED Active

  • 10291015 Ref 10291015

    Class IIb EUDAMED Active

  • 10310012 Ref 10310012

    Class IIb EUDAMED Active

  • 10312011 Ref 10312011

    Class IIb EUDAMED Active

  • 10278014 Ref 10278014

    Class IIb EUDAMED Active

  • 10271011 Ref 10271011

    Class IIb EUDAMED Active

  • 10322014 Ref 10322014

    Class IIb EUDAMED Active

  • 10310011 Ref 10310011

    Class IIb EUDAMED Active

  • 10331014 Ref 10331014

    Class IIb EUDAMED Active

  • 10291014 Ref 10291014

    Class IIb EUDAMED Active

  • 10311015 Ref 10311015

    Class IIb EUDAMED Active

  • 10330014 Ref 10330014

    Class IIb EUDAMED Active

  • 10292012 Ref 10292012

    Class IIb EUDAMED Active

  • 10290014 Ref 10290014

    Class IIb EUDAMED Active

  • 10272014 Ref 10272014

    Class IIb EUDAMED Active

  • 10271012 Ref 10271012

    Class IIb EUDAMED Active

  • 10290011 Ref 10290011

    Class IIb EUDAMED Active

  • 10292015 Ref 10292015

    Class IIb EUDAMED Active

  • 10272011 Ref 10272011

    Class IIb EUDAMED Active

  • 10311014 Ref 10311014

    Class IIb EUDAMED Active

  • 10271514 Ref 10271514

    Class IIb EUDAMED Active

  • 10272012 Ref 10272012

    Class IIb EUDAMED Active

  • 10292011 Ref 10292011

    Class IIb EUDAMED Active

  • 10271014 Ref 10271014

    Class IIb EUDAMED Active

  • 10292014 Ref 10292014

    Class IIb EUDAMED Active

  • Healon Endocoat Pro Ref 10301012

    Class IIb EUDAMED Active

  • Healon Duet Pro Ii Ref 10301016

    Class IIb EUDAMED Active

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

Notified body 0344 1 certificate

  • 2253736CE01 Supplemented

    Quality management system EU MDR

    Issued
    20 Feb 2026
    Expires
    1 Apr 2030
    Reason
    Add device or group

Related companies

Notified bodies

  • Notified body 0344

Information

Country
Sweden
Address
7, Rapsgatan, Uppsala, Sweden
Phone
+46 18 166 700
PRRC contact
Ana Roth
EUDAMED SRN
SE-MF-000017467
FDA FEI number
3004750704