A non-sterile, manual device designed to compress a piece of medical device tubing or tubular container to reversibly occlude its lumen and stop the flow of material within; it is not intended for patient-contact. It has a manual mechanism (e.g., hinging, roll
| Company | Devices | Share |
|---|---|---|
| Molded Products, Inc. | 23 | 13% |
| Surtex Instruments Ltd. | 15 | 8% |
| Integra Lifesciences Production Corporation | 13 | 7% |
| Teleflex Incorporated | 12 | 7% |
| Medicon Eg. Chirurgiemechaniker-Genossenschaft | 10 | 6% |
| Boss Instruments, Ltd., Inc. | 9 | 5% |
| Sontec Instruments, Inc. | 9 | 5% |
| Anmuth Medical International, Llc | 9 | 5% |
| Wexler Surgical, Inc. | 8 | 4% |
| Rz-Medizintechnik Gmbh | 7 | 4% |
| Hnm Stainless, Llc. | 6 | 3% |
| Novo Surgical, Inc. | 6 | 3% |
Company = labeler of record on GUDID. 32 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 |
|---|---|---|
| GDJ | CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY | 44 |
| GEN | Forceps, General & Plastic Surgery | 30 |
| GEN | FORCEPS, GENERAL & PLASTIC SURGERY | 25 |
| GDJ | Clamp, Surgical, General & Plastic Surgery | 23 |
| HTD | FORCEPS | 13 |
| HXD | Clamp | 10 |
Use these as the dimensions to specify in a tender line.
178 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Medical tubing clip/clamp, temporary, non-calibrated, reusable", from 32 companies. The largest labeler is Molded Products, Inc. with 13% of records.
GDJ (CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY), GEN (Forceps, General & Plastic Surgery), GEN (FORCEPS, GENERAL & PLASTIC SURGERY), GDJ (Clamp, Surgical, 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.