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Trauma Seal TS-iX-37

by LifeScience PLUS, Inc.

Trauma Seal TS-iX-37 is a device classified as Unclassified made by LifeScience PLUS, Inc., listed in FDA GUDID since 16 Oct 2026 (UDI-DI 00850744001456), registry data as of 2 Nov 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 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850744001456 UDI-DI Date16 Oct 2026ListedStatusListed 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  • Withdrawn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
Trauma Seal
Generic name
Plant polysaccharide haemostatic agent, non-bioabsorbable, non-antimicrobial
Model / reference
TS-iX-37
Primary DI / UDI-DI
00850744001456
FDA product code
QSY
GMDN term
Plant polysaccharide haemostatic agent, non-bioabsorbable, non-antimicrobial
Device class
U
GUDID distribution status
In Commercial Distribution
Sterilisation method
Radiation Sterilization

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
  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)