A hand-held surgical instrument designed to manually excise (strip by stab avulsion) a length or section of a vein from a patient, typically varicose veins [superficial dilated tortuous veins especially of the legs (greater saphenous veins)]. It is typically d
| Company | Devices | Share |
|---|---|---|
| Integra Lifesciences Production Corporation | 83 | 35% |
| Sklar Corporation | 23 | 10% |
| Peak Medical Distribution Inc. | 20 | 9% |
| Aesculap Ag | 18 | 8% |
| Surtex Instruments Ltd. | 11 | 5% |
| Rz-Medizintechnik Gmbh | 11 | 5% |
| Hermann Medizintechnik Gmbh | 9 | 4% |
| Medicon Eg. Chirurgiemechaniker-Genossenschaft | 9 | 4% |
| Avalign Technologies, Inc. | 9 | 4% |
| Novo Surgical, Inc. | 7 | 3% |
| Hayden Medical, Inc. | 6 | 3% |
| Steris Corporation | 6 | 3% |
Company = labeler of record on GUDID. 20 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 |
|---|---|---|
| GAI | STRIPPER, VEIN, REUSABLE | 157 |
| GAI | Stripper, Vein, Reusable | 28 |
| DWS | Instruments, Surgical, Cardiovascular | 20 |
| MDM | INSTRUMENT, MANUAL, SURGICAL, GENERAL USE | 16 |
| HRT | STRIPPER, SURGICAL | 9 |
| GDI | DISSECTOR, SURGICAL, GENERAL & PLASTIC SURGERY | 9 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
234 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Vein stripper, reusable", from 20 companies. The largest labeler is Integra Lifesciences Production Corporation with 35% of records.
GAI (STRIPPER, VEIN, REUSABLE), GAI (Stripper, Vein, Reusable), DWS (Instruments, Surgical, Cardiovascular), MDM (INSTRUMENT, MANUAL, SURGICAL, GENERAL USE)
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.