Phoenix PP22G500
Phoenix PP22G500 is a Class II device made by Dr.japan Co., Ltd., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 44900719313177), 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 | Number44900719313177 | Date24 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 44900719313177
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Phoenix
- Generic name
- Spinal needle, single-use
- Model / reference
- PP22G500
- Primary DI / UDI-DI
- 44900719313177
- FDA product code
- BSP
- GMDN term
- Spinal needle, single-use
- Device class
- Class II
- Regulation number
- 868.5150
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
- Size
- Length — 5 InchNeedle Gauge — 22 Gauge
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