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AngioSystems SorbX SX8222

by Angiosystems, Incorporated

AngioSystems SorbX SX8222 is a Class I device made by Angiosystems, Incorporated, listed in FDA GUDID since 5 Feb 2018 (UDI-DI 00816611022603), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816611022603 UDI-DI Date5 Feb 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
AngioSystems SorbX
Generic name
Radiation shielding material, ionizing
Model / reference
SX8222
Primary DI / UDI-DI
00816611022603
FDA product code
KPY
GMDN term
Radiation shielding material, ionizing
Device class
Class I
Regulation number
892.6500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Radiation shielding material, ionizing

Other devices from Angiosystems, Incorporated

See all devices from Angiosystems, Incorporated →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)