AngioSystems SorbX SX8120
AngioSystems SorbX SX8120 is a Class I device made by Angiosystems, Incorporated, listed in FDA GUDID since 5 Feb 2018 (UDI-DI 00816611022399), 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 | Number00816611022399 | Date5 Feb 2018 | StatusListed |
Official records
- AccessGUDID record 00816611022399
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- AngioSystems SorbX
- Generic name
- Patient radiation shielding pad/drape, single-use
- Model / reference
- SX8120
- Primary DI / UDI-DI
- 00816611022399
- FDA product code
- KPY
- GMDN term
- Patient radiation shielding pad/drape, single-use
- Device class
- Class I
- Regulation number
- 892.6500
- GUDID distribution status
- In Commercial Distribution
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