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Device Explorer · FDA GUDID · GMDN 38654

Arthroscopic shaver system blade, reusable

A cutting device designed for use in a powered arthroscopic shaver system handpiece (not included) for bone and soft-tissue resection during arthroscopic surgery on a joint (e.g., a knee, shoulder, or ankle). It is locked into the handpiece, and typically cons

US‑registered devices203in commercial distribution
Companies7labelers on GUDID
Single‑use43%of device records
Sterile4%labelled sterile
Prescription47%Rx‑only share
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Share of device records

Eberle Gmbh & Co. Kg10753%
Dewimed Medizintechnik Gmbh4723%
Karl Storz Gmbh & Co. Kg2713%
Conmed Corporation105%
Astura Medical94%
Arthrex, Inc.21%
Innovative Endoscopy Components, L.L.C.10%

Top labelers

CompanyDevicesShare
Eberle Gmbh & Co. Kg10753%
Dewimed Medizintechnik Gmbh4723%
Karl Storz Gmbh & Co. Kg2713%
Conmed Corporation105%
Astura Medical94%
Arthrex, Inc.21%
Innovative Endoscopy Components, L.L.C.10%

Company = labeler of record on GUDID. 7 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

REMA Shaver BladesEBERLEN/AEberle Shaver Bladesn.a.SLOTTED WHISKERArthrex®EL CAPITANEberleENDURA GATORENDURA CUDAENDURANA

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

FDA product codes

CodeNameDevices
HRXArthroscope136
HRXARTHROSCOPE36
LHXTrousers, anti-shock12
OVDIntervertebral Fusion Device With Integrated Fixation, Lumba9
HWEINSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCES9
HXRSpatula, Orthopedic7

GMDN & GCC registration

  • GMDN code 38654 · non‑implantable
  • Single‑use 43% · sterile 4% · Rx‑only 47% · 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

Width (Millimeter) · 9Outer Diameter (Millimeter) · 9Length (Millimeter) · 1

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

How many arthroscopic shaver system blade, reusable products are registered in the US?

203 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Arthroscopic shaver system blade, reusable", from 7 companies. The largest labeler is Eberle Gmbh & Co. Kg with 53% of records.

Which FDA product codes apply?

HRX (Arthroscope), HRX (ARTHROSCOPE), LHX (Trousers, anti-shock), OVD (Intervertebral Fusion Device With Integrated Fixation, Lumba)

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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