Jelco

GUDID 10351688069788

Hypodermic needle, single-use

Primary Device ID	10351688069788
NIH Device Record Key	ec1c0494-166a-4e41-b29e-f560c6bedbbf
Commercial Distribution Status	In Commercial Distribution
Brand Name	Jelco
Version Model Number	401810
Company DUNS	137835299
Company Name	SMITHS MEDICAL ASD, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00351688069781 [Primary]
GS1	10351688069788 [Package] Contains: 00351688069781 Package: BOX [100 Units] In Commercial Distribution
GS1	30351688069782 [Package] Package: CASE [10 Units] In Commercial Distribution

FMI	Needle, hypodermic, single lumen

Steralize Prior To Use	false
Device Is Sterile	true

Mark Image Registration \| Serial	Company Trademark Application Date
JELCO 97501738 not registered Live/Pending	JELCO, INC 2022-07-13
JELCO 88904643 not registered Live/Pending	Smiths Medical ASD, Inc. 2020-05-07
JELCO 88477098 not registered Live/Pending	J. E. LORTIE COMPANY LIMITED 2019-06-17
JELCO 81001492 1001492 Dead/Cancelled	Johnson & Johnson 0000-00-00
JELCO 77770940 3746512 Live/Registered	Smiths Medical ASD, Inc. 2009-06-30
JELCO 75242787 2172522 Dead/Cancelled	JELCO, INC. 1997-02-18
JELCO 73130068 1085415 Live/Registered	JOHNSON & JOHNSON 1977-06-13
JELCO 72438236 0979039 Live/Registered	JOHNSON & JOHNSON 1972-10-13
JELCO 72211073 0797327 Live/Registered	JOHNSON & JOHNSON 1965-02-01
JELCO 72166482 0767143 Dead/Expired	PETRI-KINE CAMERA COMPANY, INC. 1963-04-10