Kendall 40000032
Kendall 40000032 is a Class II device made by Cardinalhealth, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10884521081123), 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 | Number10884521081123 | Date24 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 10884521081123
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Kendall
- Generic name
- Foetal scalp electrode, spiral
- Model / Ref / Catalog
- 40000032
- Primary DI / UDI-DI
- 10884521081123
- FDA product code
- HGP
- GMDN term
- Foetal scalp electrode, spiral
- Device class
- Class II
- Regulation number
- 884.2675
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code HGP (ELECTRODE, CIRCULAR (SPIRAL), SCALP AND APPLICATOR).
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- CR SPIRAL ELECTRODE by Neward Enterprises, Inc.
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