Consulting Wallah › Device Explorer › Procedure kits & trays › Arthroscopic surgical procedure kit, medicated
Device Explorer · FDA GUDID · GMDN 44090

Arthroscopic surgical procedure kit, medicated

A collection of various sterile surgical and endoscopic instruments, dressings, pharmaceuticals, and the necessary materials used to perform an arthroscopic surgical procedure. This is a single-use device.

US‑registered devices7,000in commercial distribution
Companies2labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription99%Rx‑only share
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Share of device records

Cardinal Health 200, Llc6,92899%
Medacta International Sa721%

Top labelers

CompanyDevicesShare
Cardinal Health 200, Llc6,92899%
Medacta International Sa721%

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

Brand names on the register (sample)

CARDINAL HEALTHSportsMed InstrumentsSports Med InstrumentsSportMeds Instruments

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

FDA product codes

CodeNameDevices
OJHOrthopedic tray6,891
NBHAccessories, Arthroscopic69
NWUEndoscope introducer kit12
FDElaparoscopy kit6
OHDGynecological laparoscopic kit5
OJAIntravenous extension tubing set5

GMDN & GCC registration

  • GMDN code 44090 · non‑implantable
  • Single‑use 100% · sterile 100% · 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

No structured size data on the register.

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

How many arthroscopic surgical procedure kit, medicated products are registered in the US?

7,000 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Arthroscopic surgical procedure kit, medicated", from 2 companies. The largest labeler is Cardinal Health 200, Llc with 99% of records.

Which FDA product codes apply?

OJH (Orthopedic tray), NBH (Accessories, Arthroscopic), NWU (Endoscope introducer kit), FDE (laparoscopy kit)

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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