Primary Device ID | 30351688065586 |
NIH Device Record Key | 38fc9a62-b944-4ff1-a90b-df29ae879e1f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Jelco |
Version Model Number | 96004 |
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 | 00351688065585 [Primary] |
GS1 | 30351688065586 [Package] Contains: 00351688065585 Package: CASE [50 Units] In Commercial Distribution |
JKA | Tubes, vials, systems, serum separators, blood collection |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-04-23 |
Device Publish Date | 2017-01-09 |
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 |