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Device Explorer · FDA GUDID · GMDN 47415

Laparoscopic blunt dissector

A sterile, rigid, manual instrument designed to facilitate blunt dissection between tissue planes during laparoscopic procedures, and may additionally be used during open surgical interventions of the abdomen. It is typically made of high-grade stainless steel

US‑registered devices85in commercial distribution
Companies10labelers on GUDID
Single‑use49%of device records
Sterile45%labelled sterile
Prescription99%Rx‑only share
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Share of device records

Steris Corporation4148%
Medrobotics Corporation1315%
Deroyal Industries, Inc.1315%
Medline Industries, Inc.911%
Conmed Corporation22%
Teleflex Incorporated22%
Ethicon Endo-Surgery, Llc22%
Surgical Innovations Limited11%

Top labelers

CompanyDevicesShare
Steris Corporation4148%
Medrobotics Corporation1315%
Deroyal Industries, Inc.1315%
Medline Industries, Inc.911%
Conmed Corporation22%
Teleflex Incorporated22%
Ethicon Endo-Surgery, Llc22%
Surgical Innovations Limited11%
Smith & Nephew, Inc.11%
Endoplus11%

Company = labeler of record on GUDID. 10 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

LogiFlex - Laparoscopic Instrument SystemN/AFlexFLEXEndoplusDeRoyalCORE DYNAMICSWECKPERCUVANCEMEDLINEMedlineMEDLINE RENEWALSnowden-PencerENDOPATH

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

FDA product codes

CodeNameDevices
GCJLaparoscope, general & plastic surgery55
GCJLaparoscope, General & Plastic Surgery16
NUJElectrosurgical, cutting & coagulation accessories, laparosc15
GDIDISSECTOR, SURGICAL, GENERAL & PLASTIC SURGERY11
NLQSingle-use reprocessed ultrasonic surgical instruments8
GEIElectrosurgical, cutting & coagulation & accessories4

GMDN & GCC registration

  • GMDN code 47415 · non‑implantable
  • Single‑use 49% · sterile 45% · Rx‑only 99% · 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

Outer Diameter (Millimeter) · 5Length (Centimeter) · 4Length (Inch) · 4Width (Inch) · 2Depth (Inch) · 1

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

How many laparoscopic blunt dissector products are registered in the US?

85 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Laparoscopic blunt dissector", from 10 companies. The largest labeler is Steris Corporation with 48% of records.

Which FDA product codes apply?

GCJ (Laparoscope, general & plastic surgery), GCJ (Laparoscope, General & Plastic Surgery), NUJ (Electrosurgical, cutting & coagulation accessories, laparosc), GDI (DISSECTOR, SURGICAL, GENERAL & PLASTIC SURGERY)

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.

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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.

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