A sterile, sharp bevel-edged, hollow tubular metal instrument, combined with a Luer connector containing an absorbent foam pad, intended to be used for the collection of a biopsy specimen by fine needle aspiration (FNA) and to enable cells in a fluid specimen
| Company | Devices | Share |
|---|---|---|
| Zhejiang Curaway Medical Technology Co., Ltd. | 740 | 96% |
| Bard Peripheral Vascular, Inc. | 17 | 2% |
| Customed Inc | 12 | 2% |
| H.S. Hospital Service Spa | 2 | 0% |
Company = labeler of record on GUDID. 4 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 |
|---|---|---|
| KNW | Instrument, Biopsy | 752 |
| KNW | INSTRUMENT, BIOPSY | 36 |
| GAA | Needle, Aspiration And Injection, Disposable | 24 |
| GAA | NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE | 17 |
| GDF | GUIDE, NEEDLE, SURGICAL | 10 |
Use these as the dimensions to specify in a tender line.
771 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cell-block cytology aspiration needle", from 4 companies. The largest labeler is Zhejiang Curaway Medical Technology Co., Ltd. with 96% of records.
KNW (Instrument, Biopsy), KNW (INSTRUMENT, BIOPSY), GAA (Needle, Aspiration And Injection, Disposable), GAA (NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE)
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.