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X-Wash 80090

by Thermogenesis Corp.

X-Wash 80090 is a Class I device made by Thermogenesis Corp., listed in FDA GUDID since 4 Oct 2021 (UDI-DI 00886368000995), 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 Number00886368000995 UDI-DI Date4 Oct 2021ListedStatusListed 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  • Withdrawn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
X-Wash
Generic name
Blood centrifugation system containment kit
Model / reference
80090
Primary DI / UDI-DI
00886368000995
FDA product code
LXG
GMDN term
Blood centrifugation system containment kit
Device class
Class I
Regulation number
862.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood centrifugation system containment kit

Similar devices

Other devices filed under FDA product code LXG (Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use).

Other devices from Thermogenesis Corp.

See all devices from Thermogenesis Corp. →

Properties

  • Convenience kit
  • Combination product
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)