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BloodSTOP BS-09

by LifeScience PLUS, Inc.

BloodSTOP BS-09 is a device classified as Unclassified made by LifeScience PLUS, Inc., listed in FDA GUDID since 8 Dec 2022 (UDI-DI 00850744001098), 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 Number00850744001098 UDI-DI Date8 Dec 2022ListedStatusListed 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  • Withdrawn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 / Ref / Catalog
BS-09
Primary DI / UDI-DI
00850744001098
FDA product code
FRO
GMDN term
Plant polysaccharide haemostatic agent, non-bioabsorbable, non-antimicrobial
Device class
U
GUDID distribution status
In Commercial Distribution
Size
Area/Surface Area — 1 Square inch

Related devices

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

Similar devices

Other devices filed under FDA product code FRO (Dressing, Wound, Drug).

Other devices from LifeScience PLUS, Inc.

See all devices from LifeScience PLUS, Inc. →

Properties

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