BoneScalpel BCM-HP KIT
by Misonix, LLC
BoneScalpel BCM-HP KIT is a device classified as Unclassified made by Misonix, LLC, listed in FDA GUDID since 28 Nov 2017 (UDI-DI 00841626102057), 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 | Number00841626102057 | Date28 Nov 2017 | StatusListed |
Official records
- AccessGUDID record 00841626102057
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- BoneScalpel
- Generic name
- Hard-tissue ultrasonic surgical system handpiece
- Model / reference
- BCM-HP KIT
- Primary DI / UDI-DI
- 00841626102057
- FDA product code
- LFL
- GMDN term
- Hard-tissue ultrasonic surgical system handpiece
- Device class
- U
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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