HealthMart

GUDID 20357515191315

ULTIMED, INC.

Autoinjector needle Autoinjector needle
Primary Device ID20357515191315
NIH Device Record Key2c3068c8-8b3d-49a4-854c-b3535e296286
Commercial Distribution StatusIn Commercial Distribution
Brand NameHealthMart
Version Model Number3919131
Company DUNS024723541
Company NameULTIMED, INC.
Device Count50
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 Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100357515710055 [Unit of Use]
GS120357515191315 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FMINeedle, Hypodermic, Single Lumen

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-24

On-Brand Devices [HealthMart]

203575151913153919131
203575151912303919123
203575151709832717098

Trademark Results [HealthMart]

Mark Image

Registration | Serial
Company
Trademark
Application Date
HEALTHMART
HEALTHMART
78120650 not registered Dead/Abandoned
Elder, Roger B.
2002-04-10
HEALTHMART
HEALTHMART
75575773 not registered Dead/Abandoned
Giannini, Daniel N.
1998-10-22

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.