A sterile, manual surgical instrument designed to cut a circular or elliptical plug of tissue from the wall of the aorta to create an anastomosis site during vascular surgery. It consists of a pointed, cone-shaped, disk-like tip on the end of a plunger that is
| Company | Devices | Share |
|---|---|---|
| Teleflex Incorporated | 126 | 44% |
| Scanlan International Inc | 45 | 16% |
| Medtronic, Inc. | 40 | 14% |
| Quest Medical Inc | 35 | 12% |
| A & E Medical Corporation | 24 | 8% |
| Wexler Surgical, Inc. | 16 | 6% |
| Maquet Cardiovascular Llc | 2 | 1% |
Company = labeler of record on GUDID. 7 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 |
|---|---|---|
| DWS | INSTRUMENTS, SURGICAL, CARDIOVASCULAR | 166 |
| DWS | Instruments, Surgical, Cardiovascular | 76 |
| KDC | Instrument, Surgical, Disposable | 36 |
| LRY | Punch, Surgical | 24 |
| FZT | Cutter, Surgical | 2 |
Use these as the dimensions to specify in a tender line.
288 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Aorta punch, single-use", from 7 companies. The largest labeler is Teleflex Incorporated with 44% of records.
DWS (INSTRUMENTS, SURGICAL, CARDIOVASCULAR), DWS (Instruments, Surgical, Cardiovascular), KDC (Instrument, Surgical, Disposable), LRY (Punch, Surgical)
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.