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mo-Vis

FDA UDI

Class I (US FDA UDI)

by mo-Vis

Identity

Trade Name
mo-Vis FDA UDI
Generic Name
Assistive input-control operation training device, selection techniques FDA UDI
Device Name
Twister Bended Tube (1500 mm) Yellow FDA UDI
Model / Reference
P005-52 FDA UDI
Description
Twister Bended Tube (1500 mm) Yellow FDA UDI

Identifiers

Primary DI / UDI-DI
05407008320300 FDA UDI
FDA Product Code
KNN FDA UDI
GMDN Term
Assistive input-control operation training device, selection techniques FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3920 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Assistive input-control operation training device, selection techniques

mo-Vis by mo-Vis — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assistive input-control operation training device, selection techniques.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
mo-Vis

Sources (1)

  • FDA UDI 82ef7612-fd87-421a-9649-90ed08eae2d4 33 fields · synced May 30, 2026