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Computer-Assisted Personalized Sedation System
FDA product code PDR · Class 3 · Unknown
16
Registered devices
13
Adverse events
1
Recalls
0
510(k) clearances
Devices with this code
SEDASYS — ETHICON ENDO-SURGERY, INC.SEDASYS — ETHICON ENDO-SURGERY, INC.SEDASYS — ETHICON ENDO-SURGERY, INC.SEDASYS — ETHICON ENDO-SURGERY, INC.SEDASYS — ETHICON ENDO-SURGERY, INC.SEDASYS — ETHICON ENDO-SURGERY, INC.SEDASYS — ETHICON ENDO-SURGERY, INC.SEDASYS — ETHICON ENDO-SURGERY, INC.SEDASYS — ETHICON ENDO-SURGERY, INC.SEDASYS — ETHICON ENDO-SURGERY, INC.SEDASYS — ETHICON ENDO-SURGERY, INC.SEDASYS — ETHICON ENDO-SURGERY, INC.SEDASYS — ETHICON ENDO-SURGERY, INC.SEDASYS — ETHICON ENDO-SURGERY, INC.SEDASYS — ETHICON ENDO-SURGERY, INC.SEDASYS — ETHICON ENDO-SURGERY, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-05-13 | Ethicon Endo-Surgery Inc | Ethicon has found that disinfecting methods not specified in the Instructions For Use (IFU) have led to the degradation of the plastic material of the SEDASYS S |
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