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Velocity Alpha ™

FDA UDI

Class II (US FDA UDI)

by adeor Medical AG

Identity

Trade Name
VELOCITY ALPHA ™ FDA UDI
Generic Name
Multi-purpose surgical power tool system, line-powered FDA UDI
Model / Reference
straight nosepiece extra short FDA UDI

Identifiers

Catalog Number
VMN-XS FDA UDI
Primary DI / UDI-DI
04251388955437 FDA UDI
510(k) Number
K191479 FDA UDI
FDA Product Code
HBE FDA UDI
GMDN Term
Multi-purpose surgical power tool system, line-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4310 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

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Multi-purpose surgical power tool system, line-powered

Velocity Alpha ™ by adeor Medical AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-purpose surgical power tool system, line-powered.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
adeor Medical AG

Sources (1)

  • FDA UDI 5ec5947e-fb0e-46af-bfba-256e7d97f26e 34 fields · synced May 30, 2026