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Minitube AB

Active in EUDAMED

Swedenfrom SRN EUDAMED FDA SRN SE-MF-000002089 FEI 3001697252

Devices
34
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI

What Minitube AB makes

Minitube AB manufactures single-use medical equipment and instrument drapes, including protective sleeves and barrier sleeves for dental and medical devices such as the MIXPAC Protective Sleeve, OdneClean, VALO™ Barrier Sleeves, DentaSleeve size XL, Top Dent Sensorskydd Strl 1, Minitube Dentasleeve Protective Barrier Sleeves, Disposable infection control barrier, and Bluephase Schutzhüllen (G2).

These devices are classified as Class I and Class II medical devices and are listed in the EUDAMED, FDA 510(k), and FDA UDI registries. The company is based in Sweden (SE).

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue34

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Company details

EUDAMED SRN
SE-MF-000002089
FDA FEI number
3001697252
DUNS number
775295061
EU VAT number
SE556716406501
EUDAMED status
Active
EUDAMED registered name
Minitube AB
Registered address
44, Byvägen, 83596, Trångsviken, Sweden
PRRC contact
Bengt Myhrman(public in EUDAMED)

Frequently asked questions

How many devices does Minitube AB have in the registry?

The registry currently lists 34 devices for Minitube AB. Devices recorded under merged duplicate company entries are counted once.

Which registries list Minitube AB's devices?

Among its 34 most recently registered devices, Minitube AB has devices listed in EUDAMED (26 devices), FDA 510(k) (1 device) and FDA GUDID (13 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Minitube AB's devices fall under?

Among its 34 most recently registered devices, the classes recorded for Minitube AB's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Minitube AB in the registry?

The most recently registered devices listed for Minitube AB include OptiClear Sleeves 448800, OptiClear Sleeves 448806, OptiClear Sleeves 448804 and OptiClear Sleeves 448808.

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