Phasor Drill 008-1048
by Biotex, Inc.
Phasor Drill 008-1048 (PH-270-210), a craniotomy power tool system (FDA Class II) made by Biotex, Inc., was listed in FDA GUDID on 6 Dec 2019 (UDI-DI M710PH2702100); the registry lists it as not in commercial distribution (GUDID) 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 | NumberM710PH2702100 | Date6 Dec 2019 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Phasor Drill
- Generic name
- Craniotomy power tool system, battery-powered, single-use
- Model / Ref / Catalog
- 008-1048, PH-270-210
- Primary DI / UDI-DI
- M710PH2702100
- FDA product code
- HBE, KIJ, GFG
- GMDN term
- Craniotomy power tool system, battery-powered, single-use
- Device class
- Class II
- Regulation number
- 882.4310, 878.4820
- GUDID distribution status
- Not in Commercial Distribution
- MRI safety
- MR Unsafe
- Size
- Outer Diameter — 2.7 Millimeter
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