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Cyberwand

FDA UDI

Class II (US FDA UDI)

by Gyrus Acmi, Inc.

Identity

Trade Name
CYBERWAND FDA UDI
Generic Name
Electrohydraulic lithotripsy system FDA UDI
Device Name
CYBERWAND PROBE SET (USL Renal/Bladder Probe) (3/PK) FDA UDI
Model / Reference
CW-RBPBX FDA UDI
Description
CYBERWAND PROBE SET (USL Renal/Bladder Probe) (3/PK) FDA UDI

Identifiers

Primary DI / UDI-DI
00821925044173 FDA UDI
510(k) Number
K120303 FDA UDI
FDA Product Code
FFK FDA UDI
GMDN Term
Electrohydraulic lithotripsy system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4480 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrohydraulic lithotripsy system

Cyberwand by Gyrus Acmi, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrohydraulic lithotripsy system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gyrus Acmi, Inc.

Sources (1)

  • FDA UDI 9f430ce6-f8a8-44b0-837b-d797167e47c2 34 fields · synced Jun 8, 2026