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Cyber Blade

FDA UDI

Class II (US FDA UDI)

by Quanta System Spa

Identity

Trade Name
Cyber Blade FDA UDI
Generic Name
Tissue morcellation system handpiece, battery-powered FDA UDI
Device Name
Cyber Blade Morcelletor Set FDA UDI
Model / Reference
CVA000002 FDA UDI
Description
Cyber Blade Morcelletor Set FDA UDI

Identifiers

Primary DI / UDI-DI
08059173391707 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Tissue morcellation system handpiece, battery-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tissue morcellation system handpiece, battery-powered

Cyber Blade by Quanta System Spa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue morcellation system handpiece, battery-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Quanta System Spa

Sources (1)

  • FDA UDI a4723890-d1cc-4a34-89c6-25f3fd4e06b8 33 fields · synced Jun 8, 2026