A device or collection of devices that includes a flexible polymer tube intended to be used primarily to transfer gametes (eggs or sperm) and/or embryos into the female reproductive tract for the purpose of assisted reproduction [e.g., intrauterine inseminatio
| Company | Devices | Share |
|---|---|---|
| Kitazato Corporation | 103 | 37% |
| Cook Incorporated | 61 | 22% |
| Coopersurgical, Inc. | 28 | 10% |
| Allwin Medical Devices, Inc. | 27 | 10% |
| Laboratoire Ccd | 10 | 4% |
| Gynetics Medical Products Nv | 9 | 3% |
| C R I | 8 | 3% |
| Guangzhou Hehong Biotech Co., Ltd. | 6 | 2% |
| Shenzhen Vitavitro Biotech Co.,Ltd. | 5 | 2% |
| Labotect Labor-Technik Göttingen Gesellschaft Mit Beschränkter Haftung | 5 | 2% |
| Origio A/S | 5 | 2% |
| Femasys Inc. | 4 | 1% |
Company = labeler of record on GUDID. 14 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 |
|---|---|---|
| MQF | CATHETER, ASSISTED REPRODUCTION | 197 |
| MQF | Catheter, Assisted Reproduction | 85 |
| MFD | Cannula, Intrauterine Insemination | 19 |
| HDR | CAP, CERVICAL | 14 |
| MFD | CANNULA, INTRAUTERINE INSEMINATION | 10 |
| KNA | Instrument, Manual, Specialized Obstetric-Gynecologic | 2 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
275 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Assisted reproduction transfer catheter/set", from 14 companies. The largest labeler is Kitazato Corporation with 37% of records.
MQF (CATHETER, ASSISTED REPRODUCTION), MQF (Catheter, Assisted Reproduction), MFD (Cannula, Intrauterine Insemination), HDR (CAP, CERVICAL)
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.