A hand-held manual instrument intended to be used by a physician for the extraction of an intrauterine device (IUD). The proximal end forms a handle which may vary in shape and which tapers toward the distal end to form a hook. It is typically made of high-gra
| Company | Devices | Share |
|---|---|---|
| Gynex Corporation | 8 | 16% |
| Novo Surgical, Inc. | 6 | 12% |
| Hnm Stainless, Llc. | 4 | 8% |
| Integra Lifesciences Production Corporation | 4 | 8% |
| Rz-Medizintechnik Gmbh | 3 | 6% |
| Hayden Medical, Inc. | 3 | 6% |
| Br Surgical, Llc | 3 | 6% |
| Avalign Technologies, Inc. | 3 | 6% |
| Panpac Medical Corporation | 2 | 4% |
| Coopersurgical, Inc. | 2 | 4% |
| Marina Medical Instruments, Inc. | 2 | 4% |
| Surgical Direct, Inc. | 2 | 4% |
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 |
|---|---|---|
| HHF | Remover, Intrauterine Device, Contraceptive, Hook-Type | 24 |
| HHF | REMOVER, INTRAUTERINE DEVICE, CONTRACEPTIVE, HOOK-TYPE | 14 |
| FHQ | HOLDER, NEEDLE, GASTROENTEROLOGIC | 3 |
| MDM | Instrument, Manual, Surgical, General Use | 2 |
| GDG | Hook, Surgical, General & Plastic Surgery | 2 |
| KOH | INSTRUMENT, MANUAL, GENERAL OBSTETRIC-GYNECOLOGIC | 1 |
Use these as the dimensions to specify in a tender line.
50 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Intrauterine device removal hook, reusable", from 20 companies. The largest labeler is Gynex Corporation with 16% of records.
HHF (Remover, Intrauterine Device, Contraceptive, Hook-Type), HHF (REMOVER, INTRAUTERINE DEVICE, CONTRACEPTIVE, HOOK-TYPE), FHQ (HOLDER, NEEDLE, GASTROENTEROLOGIC), 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.