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BloodSTOP 832230

by LifeScience PLUS, Inc.

BloodSTOP 832230 is a device classified as Unclassified made by LifeScience PLUS, Inc., listed in FDA GUDID since 10 Jul 2024 (UDI-DI 00850744001609), 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 Number00850744001609 UDI-DI Date10 Jul 2024ListedStatusListed 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  • Withdrawn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
BloodSTOP
Generic name
Plant polysaccharide haemostatic agent, non-bioabsorbable, non-antimicrobial
Model / reference
832230
Primary DI / UDI-DI
00850744001609
FDA product code
QSY
GMDN term
Plant polysaccharide haemostatic agent, non-bioabsorbable, non-antimicrobial
Device class
U
GUDID distribution status
In Commercial Distribution

Related devices

Category: Plant polysaccharide haemostatic agent, non-bioabsorbable, non-antimicrobial

Similar devices

Other devices filed under FDA product code QSY (Hemostatic Wound Dressing Without Thrombin Or Other Biologics).

Other devices from LifeScience PLUS, Inc.

See all devices from LifeScience PLUS, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)