Leadpoint 9013C0551
by Natus Manufacturing Limited
Leadpoint 9013C0551 is a Class II device made by Natus Manufacturing Limited, listed in FDA GUDID since 20 Mar 2019 (UDI-DI 00382830049092), registry data as of 23 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 | Number00382830049092 | Date20 Mar 2019 | StatusListed |
Official records
- AccessGUDID record 00382830049092
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Leadpoint
- Generic name
- Electromyograph
- Model / Ref / Catalog
- 9013C0551
- Primary DI / UDI-DI
- 00382830049092
- FDA product code
- IKD
- GMDN term
- Electromyograph
- Device class
- Class II
- Regulation number
- 890.1175
- GUDID distribution status
- In Commercial Distribution
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