EndoPuls 811 1650903
EndoPuls 811 1650903 (5435) is a medical device (FDA Class I; FDA product code ISA, Massager, Therapeutic, Electric) made by Zimmer MedizinSysteme GmbH, listed in FDA GUDID since 17 Mar 2025 (UDI-DI 04053815088332), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04053815088332 | Date17 Mar 2025 | StatusListed |
Official records
- AccessGUDID record 04053815088332
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- EndoPuls 811
- Generic name
- Electromechanical orthopaedic extracorporeal shock wave therapy system
- Model / Ref / Catalog
- 1650903, 5435
- Primary DI / UDI-DI
- 04053815088332
- FDA product code
- ISA
- GMDN term
- Electromechanical orthopaedic extracorporeal shock wave therapy system
- Device class
- Class I
- Regulation number
- 890.5660
- GUDID distribution status
- In Commercial Distribution
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