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Hemasorb Plus HPS-311-NS

by Abyrx, Inc.

Hemasorb Plus HPS-311-NS is a device classified as Unclassified made by Abyrx, Inc., listed in FDA GUDID since 15 Dec 2016 (UDI-DI 00850391007009), 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 Number00850391007009 UDI-DI Date15 Dec 2016ListedStatusListed 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  • Withdrawn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
Hemasorb Plus
Generic name
Bone wax, synthetic
Model / reference
HPS-311-NS
Primary DI / UDI-DI
00850391007009
FDA product code
MTJ
GMDN term
Bone wax, synthetic
Device class
U
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code MTJ (Wax,Bone).

Other devices from Abyrx, Inc.

See all devices from Abyrx, Inc. →

Properties

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