Primary Device ID | 08800186704370 |
NIH Device Record Key | 87e10717-e40b-424d-b181-b080097f6d92 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CareSens™ Pen Needle |
Version Model Number | P3204 |
Catalog Number | 32GX4mm |
Company DUNS | 694103988 |
Company Name | W.L. MED CO.,LTD. |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08800186704370 [Package] Contains: 08800186704578 Package: Inner Box [100 Units] In Commercial Distribution |
GS1 | 08800186704387 [Package] Package: Middle Box [1200 Units] In Commercial Distribution |
GS1 | 08800186704394 [Package] Contains: 08800186704387 Package: Carton Box [7200 Units] In Commercial Distribution |
GS1 | 08800186704578 [Primary] |
FMI | Needle, Hypodermic, Single Lumen |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-21 |
Device Publish Date | 2023-08-11 |
08800186704493 | P3305 |
08800186704462 | P3304 |
08800186704431 | P3206 |
08800186704400 | P3205 |
08800186704370 | P3204 |
08800186704349 | P3108 |
08800186704318 | P3106 |
08800186704288 | P3105 |
08800186704226 | P2912 |
08800186704257 | P3008 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CARESENS 79386381 not registered Live/Pending |
I-sens, Inc. 2023-08-24 |
CARESENS 78615654 3486219 Live/Registered |
i-SENS, Inc. 2005-04-25 |