Consulting Wallah › Device Explorer › Syringes, needles & infusion › Laparoscopic access cannula, reprocessed
Device Explorer · FDA GUDID · GMDN 61813

Laparoscopic access cannula, reprocessed

A sterile, single-lumen surgical device intended to be percutaneously inserted through the abdominal wall to create an access port for a laparoscope/laparoscopic instrument during laparoscopy. The cannula is often provided with a shut-off valve for gas/fluid s

US‑registered devices644in commercial distribution
Companies5labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Provision38660%
Medline Industries, Inc.23336%
Stryker Sustainability Solutions, Inc.193%
Suretek Medical41%
Grace Manufacturing, Inc.20%

Top labelers

CompanyDevicesShare
Provision38660%
Medline Industries, Inc.23336%
Stryker Sustainability Solutions, Inc.193%
Suretek Medical41%
Grace Manufacturing, Inc.20%

Company = labeler of record on GUDID. 5 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

N/ACovidienSustainable TechnologiesConmed/LinvatecDeSoutterStrykerSmith and NephewSustainable TehnologiesEthiconDePuy MitekArthrexMedtronicConMed LinvatecConMedVelocity OrthopedicsMicroPort Ortho

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

FDA product codes

CodeNameDevices
NBHAccessories, Arthroscopic323
NLMLaparoscope, General & Plastic Surgery, Reprocessed218
NBHAccessories, arthroscopic132
NLMLaparoscope, general & plastic surgery, reprocessed89
NLMLAPAROSCOPE, GENERAL & PLASTIC SURGERY, REPROCESSED80
KDCInstrument, Surgical, Disposable4

GMDN & GCC registration

  • GMDN code 61813 · non‑implantable
  • Single‑use 100% · sterile 100% · 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

Length (Millimeter) · 26Lumen/Inner Diameter (Millimeter) · 12Catheter Gauge (French) · 2

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

How many laparoscopic access cannula, reprocessed products are registered in the US?

644 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Laparoscopic access cannula, reprocessed", from 5 companies. The largest labeler is Provision with 60% of records.

Which FDA product codes apply?

NBH (Accessories, Arthroscopic), NLM (Laparoscope, General & Plastic Surgery, Reprocessed), NBH (Accessories, arthroscopic), NLM (Laparoscope, general & plastic surgery, reprocessed)

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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