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Piranha

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
PIRANHA FDA UDI
Generic Name
Tissue morcellation system handpiece, line-powered FDA UDI
Device Name
ROTATIONS-MORCELLATOR Ø 4.8MM WL 335MM for MORCESCOPE, for morcellation following laser prostate enucleation, sterile FDA UDI
Model / Reference
49700113 FDA UDI
Description
ROTATIONS-MORCELLATOR Ø 4.8MM WL 335MM for MORCESCOPE, for morcellation following laser prostate enucleation, sterile FDA UDI

Identifiers

Catalog Number
49700113 FDA UDI
Primary DI / UDI-DI
04055207063422 FDA UDI
FDA Product Code
FJL FDA UDI
GMDN Term
Tissue morcellation system handpiece, line-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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 4.8 Millimeter FDA UDI
Length — 335 Millimeter FDA UDI

Category: Tissue morcellation system handpiece, line-powered

Piranha by Richard Wolf GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Richard Wolf GmbH

Sources (1)

  • FDA UDI 41725a92-15a1-402e-a017-dac94ed66620 37 fields · synced May 30, 2026