Consulting Wallah › Device Explorer › Other devices › Tissue morcellation system handpiece, line-powered
Device Explorer · FDA GUDID · GMDN 46732

Tissue morcellation system handpiece, line-powered

A hand-held component of a tissue morcellation system intended to be used to mechanically cut (slice), core (cut a hole into), peel (remove surface), and extract selected tissue from the body during surgery. It consists of a high-speed rotating blade in a hold

US‑registered devices54in commercial distribution
Companies8labelers on GUDID
Single‑use89%of device records
Sterile89%labelled sterile
Prescription93%Rx‑only share
ShareLinkedIn

Share of device records

Nico Corporation1731%
Meditrina, Inc.1324%
Interscope, Inc1120%
Lumenis Ltd.47%
Richard Wolf Gmbh47%
Smith & Nephew, Inc.36%
Ami Agency For Medical Innovations Gmbh12%
Hologic, Inc.12%

Top labelers

CompanyDevicesShare
Nico Corporation1731%
Meditrina, Inc.1324%
Interscope, Inc1120%
Lumenis Ltd.47%
Richard Wolf Gmbh47%
Smith & Nephew, Inc.36%
Ami Agency For Medical Innovations Gmbh12%
Hologic, Inc.12%

Company = labeler of record on GUDID. 8 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

VersaCut™ HandpieceVersaCut HandpieceVersaCut+ Tissue Morcellator with Regular HandpiVersaCut+ Tissue Morcellator with Inverted Handpi-CutPIRANHATRUCLEARTM HandpieceTRUCLEARTM ULTRA Plus DeviceEndoRotor® 3.2mm Powered Endoscopic Debridement EndoRotor® 3.2mm Powered Endoscopic Debridement EndoRotor® 3.2mm Powered Endoscopic Debridement EndoRotor® 3.2mm Endoscopic Powered Resection (EEndoRotor® 3.2mm Endoscopic Powered Resection (EEndoRotor® 3.2mm Powered Endoscopic Debridement EndoRotor® 3.2mm Endoscopic Powered Resection (EEndoRotor® 3.2mm Endoscopic Powered Resection (E

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
PTEEndoscopic Morcellator Gastroenterology20
GEIElectrosurgical, Cutting & Coagulation & Accessories17
HIGInsufflator, Hysteroscopic13
HIHHysteroscope (And Accessories)13
HIHHYSTEROSCOPE (AND ACCESSORIES)5
GCJLaparoscope, General & Plastic Surgery4

GMDN & GCC registration

  • GMDN code 46732 · non‑implantable
  • Single‑use 89% · sterile 89% · Rx‑only 93% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Millimeter) · 4Outer Diameter (Millimeter) · 4

Use these as the dimensions to specify in a tender line.

How many tissue morcellation system handpiece, line-powered products are registered in the US?

54 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Tissue morcellation system handpiece, line-powered", from 8 companies. The largest labeler is Nico Corporation with 31% of records.

Which FDA product codes apply?

PTE (Endoscopic Morcellator Gastroenterology), GEI (Electrosurgical, Cutting & Coagulation & Accessories), HIG (Insufflator, Hysteroscopic), HIH (Hysteroscope (And Accessories))

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

How do I get quotes?

Add tissue morcellation system handpiece, line-powered to the RFQ basket or use the form below with quantity, specification and delivery location; the Network returns comparable quotes from verified suppliers in 2–5 working days.

Request quotes for Tissue morcellation system handpiece, line-powered

Hospitals, pharmacies and distributors anywhere: tell us what you need and the Consulting Wallah Network returns comparable quotes from verified suppliers. No fee for buyers.

Buying tissue morcellation system handpiece, line-powered for a hospital group?Free executive assessment: we benchmark your prices and tender structure against the Network.
Book the free assessment

Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

Get quotes →