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
| Company | Devices | Share |
|---|---|---|
| Provision | 809 | 44% |
| Medline Industries, Inc. | 670 | 37% |
| Suretek Medical | 278 | 15% |
| Stryker Sustainability Solutions, Inc. | 61 | 3% |
| Volmed Brasil Equipamentos Ltda | 2 | 0% |
Company = labeler of record on GUDID. 5 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| HRX | Arthroscope | 1,022 |
| HRX | ARTHROSCOPE | 341 |
| GFF | BUR, SURGICAL, GENERAL & PLASTIC SURGERY | 321 |
| NBH | Accessories, Arthroscopic | 285 |
| EQJ | BUR, EAR, NOSE AND THROAT | 15 |
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES | 14 |
Use these as the dimensions to specify in a tender line.
1,820 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Arthroscopic shaver system blade, reprocessed", from 5 companies. The largest labeler is Provision with 44% of records.
HRX (Arthroscope), HRX (ARTHROSCOPE), GFF (BUR, SURGICAL, GENERAL & PLASTIC SURGERY), NBH (Accessories, Arthroscopic)
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.
Add arthroscopic shaver system blade, reprocessed to the RFQ basket or use the form below with quantity, specification and delivery location; the Network returns comparable quotes from verified suppliers in 2–5 working days.
Hospitals, pharmacies and distributors anywhere: tell us what you need and the Consulting Wallah Network returns comparable quotes from verified suppliers. No fee for buyers.
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.