Consulting Wallah › Device Explorer › Other devices › Laparoscopic trocar blade, reprocessed
Device Explorer · FDA GUDID · GMDN 61814

Laparoscopic trocar blade, reprocessed

A rigid surgical instrument with a sharp pyramidal or conical point intended to puncture the abdominal wall to facilitate the introduction of a laparoscopic access cannula (not included) during laparoscopy. It is intended to fill the lumen of the laparoscopic

US‑registered devices57in commercial distribution
Companies2labelers on GUDID
Single‑use100%of device records
Sterile98%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Medline Industries, Inc.3765%
Stryker Sustainability Solutions, Inc.2035%

Top labelers

CompanyDevicesShare
Medline Industries, Inc.3765%
Stryker Sustainability Solutions, Inc.2035%

Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

N/AMedline ReNewal

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

FDA product codes

CodeNameDevices
NLMLAPAROSCOPE, GENERAL & PLASTIC SURGERY, REPROCESSED163
JOWSLEEVE, LIMB, COMPRESSIBLE1
GCJLaparoscope, general & plastic surgery1

GMDN & GCC registration

  • GMDN code 61814 · non‑implantable
  • Single‑use 100% · sterile 98% · Rx‑only 100% · 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

Lumen/Inner Diameter (Millimeter) · 28Length (Millimeter) · 18Circumference (Inch) · 1Outer Diameter (Millimeter) · 1

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

How many laparoscopic trocar blade, reprocessed products are registered in the US?

57 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Laparoscopic trocar blade, reprocessed", from 2 companies. The largest labeler is Medline Industries, Inc. with 65% of records.

Which FDA product codes apply?

NLM (LAPAROSCOPE, GENERAL & PLASTIC SURGERY, REPROCESSED), JOW (SLEEVE, LIMB, COMPRESSIBLE), GCJ (Laparoscope, 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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