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AngioSystems SorbX SX8120

by Angiosystems, Incorporated

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 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 Number00816611022399 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  • Withdrawn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
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

Similar devices

Other devices filed under FDA product code KPY (Shield, Protective, Personnel).

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)