HumaPen® Luxura™ HD MS9673

GUDID 00300029673019

HumaPen Luxura HD is a reusable pen injector intended for use with Lilly 3 mL insulin cartridges.

ELI LILLY AND COMPANY

Cartridge-accepting autoinjector, mechanical
Primary Device ID00300029673019
NIH Device Record Key7c4a671a-8c83-4764-bf12-20c3e8f01451
Commercial Distribution StatusIn Commercial Distribution
Brand NameHumaPen® Luxura™ HD
Version Model NumberMS9673
Catalog NumberMS9673
Company DUNS006421325
Company NameELI LILLY AND COMPANY
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-800-545-5979
Emailxxx@xxx.xxx
Phone1-800-545-5979
Emailxxx@xxx.xxx
Phone1-800-545-5979
Emailxxx@xxx.xxx
Phone1-800-545-5979
Emailxxx@xxx.xxx
Phone1-800-545-5979
Emailxxx@xxx.xxx
Phone1-800-545-5979
Emailxxx@xxx.xxx
Phone1-800-545-5979
Emailxxx@xxx.xxx
Phone1-800-545-5979
Emailxxx@xxx.xxx
Phone1-800-545-5979
Emailxxx@xxx.xxx
Phone1-800-545-5979
Emailxxx@xxx.xxx
Phone1-800-545-5979
Emailxxx@xxx.xxx
Phone1-800-545-5979
Emailxxx@xxx.xxx
Phone1-800-545-5979
Emailxxx@xxx.xxx
Phone1-800-545-5979
Emailxxx@xxx.xxx
Phone1-800-545-5979
Emailxxx@xxx.xxx

Device Identifiers

Device Issuing AgencyDevice ID
GS100300029673019 [Primary]
GS130300029673010 [Package]
Package: Case [25 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FMFSyringe, Piston

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-21

Devices Manufactured by ELI LILLY AND COMPANY

00300021283551 - Lilly Together2024-08-05 Software as a medical device (SaMD) for some Lilly medicines which provides access to medication reminders and customer support
00300021284558 - Lilly Together2024-08-05 Software as a medical device (SaMD) for some Lilly medicines which provides access to medication reminders and customer support
00300021176556 - Lilly Together2024-03-19 Software as a medical device (SaMD) for some Lilly medicines which provides access to medication reminders and customer support
00300021177553 - Lilly Together2024-03-19 Software as a medical device (SaMD) for some Lilly medicines which provides access to medication reminders and customer support
00300021174552 - Lilly Together2024-02-26 Software as a medical device (SaMD) for some Lilly medicines which provides access to medication reminders and customer support
00300021175559 - Lilly Together2024-02-26 Software as a medical device (SaMD) for some Lilly medicines which provides access to medication reminders and customer support
50300021151558 - Tempo Refill Kit2023-09-05 Tempo Refill Kit - This is a convenience kit which contains multiple devices with different counts: Lancets/Strips/BD needles an
30300020947554 - Tempo Refill Kit2023-08-24 Tempo Refill Kit - Convenience Kit for patients with diabetes, which contains lancets, testing strips, and BD needles.

Trademark Results [HumaPen]

Mark Image

Registration | Serial
Company
Trademark
Application Date
HUMAPEN
HUMAPEN
75724618 2767043 Live/Registered
Eli Lilly and Company
1999-06-09
HUMAPEN
HUMAPEN
75057332 not registered Dead/Abandoned
Eli Lilly and Company
1996-02-13
HUMAPEN
HUMAPEN
74333981 not registered Dead/Abandoned
Eli Lilly and Company
1992-11-23

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