Hemasorb Plus

GUDID 00850391007108

ABYRX, INC.

Bone wax, synthetic
Primary Device ID00850391007108
NIH Device Record Key2df891da-60c2-4004-8abe-67cc79395546
Commercial Distribution StatusIn Commercial Distribution
Brand NameHemasorb Plus
Version Model NumberHPS-811-NS
Company DUNS078818942
Company NameABYRX, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100850391007108 [Primary]

FDA Product Code

MTJWax,Bone

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-12-13

On-Brand Devices [Hemasorb Plus ]

00850391007108HPS-811-NS
00850391007009HPS-311-NS

Trademark Results [Hemasorb Plus]

Mark Image

Registration | Serial
Company
Trademark
Application Date
HEMASORB PLUS
HEMASORB PLUS
86062141 not registered Dead/Abandoned
Abyrx, Inc.
2013-09-11

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