10430BL
10430BL is a Class I device made by Karl Storz SE & CO. KG, listed in FDA GUDID since 4 Sep 2018 (UDI-DI 04048551048443), 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 | Number04048551048443 | Date4 Sep 2018 | StatusListed |
Official records
- AccessGUDID record 04048551048443
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Gastrointestinal/airway foreign body retrieval basket, single-use
- Model / reference
- 10430BL
- Primary DI / UDI-DI
- 04048551048443
- FDA product code
- LRC
- GMDN term
- Gastrointestinal/airway foreign body retrieval basket, single-use
- Device class
- Class I
- Regulation number
- 874.4420
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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