A rigid, manual, non-electrosurgical instrument intended to obtain tissue specimens during endoscopic procedures (e.g., laparoscopy, thoracoscopy, spinoscopy, arthroscopy). It is typically constructed as a long instrument with one sliding and one stationary ro
| Company | Devices | Share |
|---|---|---|
| Rz-Medizintechnik Gmbh | 218 | 23% |
| Sontec Instruments, Inc. | 98 | 10% |
| Hoogland Spine Products Gmbh | 90 | 10% |
| Elmed Incorporated | 81 | 9% |
| Doppkon Gmbh & Co. Kg | 69 | 7% |
| Avalign Technologies, Inc. | 56 | 6% |
| Joimax Gmbh | 53 | 6% |
| Sopro-Comeg Gmbh | 45 | 5% |
| Karl Storz Gmbh & Co. Kg | 44 | 5% |
| Richard Wolf Gmbh | 41 | 4% |
| Fentex Medical Gmbh | 31 | 3% |
| Gimmi Gmbh | 22 | 2% |
Company = labeler of record on GUDID. 30 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 |
|---|---|---|
| GEN | FORCEPS, GENERAL & PLASTIC SURGERY | 170 |
| GCJ | Laparoscope, General & Plastic Surgery | 98 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 90 |
| GEN | Forceps, General & Plastic Surgery | 84 |
| FCL | FORCEPS, BIOPSY, NON-ELECTRIC | 77 |
| GCJ | Laparoscope, general & plastic surgery | 67 |
Use these as the dimensions to specify in a tender line.
942 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Rigid endoscopic biopsy forceps, reusable", from 30 companies. The largest labeler is Rz-Medizintechnik Gmbh with 23% of records.
GEN (FORCEPS, GENERAL & PLASTIC SURGERY), GCJ (Laparoscope, General & Plastic Surgery), GEI (Electrosurgical, Cutting & Coagulation & Accessories), GEN (Forceps, General & Plastic Surgery)
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.