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AngioSystems SorbX SX1000

by Angiosystems, Incorporated

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816611026663 UDI-DI Date29 Sep 2026ListedStatusListed GUDID: in commercial distribution

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  • Withdrawn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 / Ref / Catalog
SX1000
Primary DI / UDI-DI
00816611026663
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

Other devices from Angiosystems, Incorporated

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Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No