Home › Device types › KDM
Sigmoidoscope, Rigid, Non-Electrical
FDA product code KDM · Class 2 · Gastroenterology, Urology
24
Registered devices
0
Adverse events
1
Recalls
1
510(k) clearances
Devices with this code
Welch Allyn, Inc. — WELCH ALLYN, INC.Rectoscope equipment — SAPI MED SPARectoscope — SAPI MED SPARectoscope equipment — SAPI MED SPAWelch Allyn, Inc. — WELCH ALLYN, INC.MONARCH DISPOSABLE ANOSCOPE — MONARCH MOLDING, INC.Rectoscope equipment — SAPI MED SPARectoscope — SAPI MED SPARectoscope — SAPI MED SPAWelch Allyn, Inc. — WELCH ALLYN, INC.Rectoscope — SAPI MED SPARectoscope equipment — SAPI MED SPAMONARCH DISPOSABLE ANOSCOPE — MONARCH MOLDING, INC.MONARCH DISPOSABLE ANOSCOPE — MONARCH MOLDING, INC.Welch Allyn, Inc. — WELCH ALLYN, INC.Rectoscope — SAPI MED SPAGrip for rectoscope — SAPI MED SPAWelch Allyn, Inc. — WELCH ALLYN, INC.Welch Allyn, Inc. — WELCH ALLYN, INC.Welch Allyn, Inc. — WELCH ALLYN, INC.Welch Allyn, Inc. — WELCH ALLYN, INC.MONARCH DISPOSABLE ANOSCOPE — MONARCH MOLDING, INC.Welch Allyn, Inc. — WELCH ALLYN, INC.Welch Allyn, Inc. — WELCH ALLYN, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-04-23 | Adler MicroMed, Inc. | Due to issue with product sterility. Sterilization service provider had falsified records. |
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