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Medtronic 3F Therapeutics, Inc.

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Devices
18

Catalogue18

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  • 3f® 1000-21

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-29

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-29

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-23

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-23

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-21

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-25

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-25

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-27

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-29

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-21

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-27

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-29

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-29

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-29

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-27

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-23

    Withdrawn Registry: GUDID Class:III
  • 3f® 1000-25

    Withdrawn Registry: GUDID Class:III

Rows 1-18 of 18

Company details

DUNS number
079527232
Phone
+1(800)633-8766

Frequently asked questions

How many devices does MEDTRONIC 3F THERAPEUTICS, INC. have in the registry?

The registry currently lists 18 devices for MEDTRONIC 3F THERAPEUTICS, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list MEDTRONIC 3F THERAPEUTICS, INC.'s devices?

Among its 18 most recently registered devices, MEDTRONIC 3F THERAPEUTICS, INC. has devices listed in FDA GUDID (18 devices).

What risk classes do MEDTRONIC 3F THERAPEUTICS, INC.'s devices fall under?

Among its 18 most recently registered devices, the classes recorded for MEDTRONIC 3F THERAPEUTICS, INC.'s devices are Class III. Each device page shows its own class and authorisation.

What are the newest devices from MEDTRONIC 3F THERAPEUTICS, INC. in the registry?

The most recently registered devices listed for MEDTRONIC 3F THERAPEUTICS, INC. include 3f® 1000-21, 3f® 1000-29, 3f® 1000-23 and 3f® 1000-25.

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