Kendall 30951555
Kendall 30951555 is a Class I device made by Cardinalhealth, listed in FDA GUDID since 27 Jun 2018 (UDI-DI 20884527010391), 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 | Number20884527010391 | Date27 Jun 2018 | StatusListed |
Official records
- AccessGUDID record 20884527010391
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Kendall
- Generic name
- Abdominal binder, single-use
- Model / Ref / Catalog
- 30951555
- Primary DI / UDI-DI
- 20884527010391
- FDA product code
- FSD
- GMDN term
- Abdominal binder, single-use
- Device class
- Class I
- Regulation number
- 880.5160
- GUDID distribution status
- In Commercial Distribution
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- MATERNITY SUPPORTER by R.G. Moore
- EARETTE HEARING AID SEARS #8054 by Oticon Corp.