MONARCH™ Stone Retrieval Basket MUR-000015
Listed
Valid until
Not applicable
FDA recalls
1 ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10810068811091 | Date4 May 2026 | StatusListed |
Recalls
-
- Ongoing Z-0052-2025
Endoscopy/bronchoscopy/urology devices may have a strain relief defect with some cart and tower power cords that may cause an electrical short, which may lead to system shutdown, which can lead to prolonged procedure or case conversion, and if the user (e.g., operating room staff) touches exposed wires or conductive fluids in contact with the exposed wires, there is a chance of electrical shock.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- MONARCH™ Stone Retrieval Basket
- Generic Name
- Urinary stone retrieval basket, single-use
- Model / Ref / Catalog
- MUR-000015
- Primary DI / UDI-DI
- 10810068811091
- 510(k) Number
- FDA Product Code
- FFL
- GMDN Term
- Urinary stone retrieval basket, single-use
- Device Class
- Class II
- Regulation Number
- 876.4680
- GUDID distribution status
- In Commercial Distribution
Other devices from Auris Health, Inc.
Properties
Other properties (8)
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No