Home › Device types › MFD
Cannula, Intrauterine Insemination
FDA product code MFD · Class 2 · Obstetrics/Gynecology
32
Registered devices
4
Adverse events
1
Recalls
29
510(k) clearances
Devices with this code
Wallace Artificial Insemination Catheter — Coopersurgical, Inc.The Inseminator — Coopersurgical, Inc.Uni-Sem — Coopersurgical, Inc.MiniSpace — Coopersurgical, Inc.Trackable Intra Uterine Insemination Catheter Open Tip — ALLWIN MEDICAL DEVICES, INC.Wallace — ICU MEDICAL, INC.Curved Intra Uterine Insemination Catheter — ALLWIN MEDICAL DEVICES, INC.Pneupac — ICU MEDICAL, INC.Trackable Intra Uterine Insemination Catheter — ALLWIN MEDICAL DEVICES, INC.Soft-Pass — COOK INCORPORATEDInsemi-Cath — COOK INCORPORATEDInsemination Cannula with Syringe — Coopersurgical, Inc.SpermSelect Curve Kit — Coopersurgical, Inc.Insemination Cannula with Syringe — Coopersurgical, Inc.Cook — COOK INCORPORATEDPivet — COOK INCORPORATEDInsemina Open Tip Intra Uterine Insemination Catheter — ALLWIN MEDICAL DEVICES, INC.Select IUI — Coopersurgical, Inc.The Inseminator — Coopersurgical, Inc.Flexi Intra Uterine Insemination Catheter Open Tip — ALLWIN MEDICAL DEVICES, INC.Soft-Pass — COOK INCORPORATEDCurved Insemina Intra Uterine Insemination Catheter Open Tip — ALLWIN MEDICAL DEVICES, INC.Insemi-Cath — COOK INCORPORATEDFlexi Intra Uterine Insemination Catheter — ALLWIN MEDICAL DEVICES, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-02-28 | CooperSurgical, Inc. | Expiration date discrepancy. Marked as 5 years. Expiration date should be 3 years. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
