Primary Device ID | 06970384250961 |
NIH Device Record Key | ff63b599-79ef-485a-9741-23fbab9ddafa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SCIAN |
Version Model Number | LD-579 |
Company DUNS | 543364560 |
Company Name | HONSUN (NANTONG) 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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
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 | 06970384250961 [Primary] |
DXN | System, Measurement, Blood-Pressure, Non-Invasive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-04-08 |
Device Publish Date | 2022-03-31 |
06970384250954 | LD-579S |
06970384250947 | LD-566S |
06970384250916 | LD-752S |
06970384250657 | LD-575S |
06970384250640 | LD-737S |
06970384250633 | LD-562S |
06970384250626 | LD-527 |
06970384250619 | LD-520 |
06970384250435 | LD-100 |
06970384250213 | LD-753S |
06970384250183 | LD521 |
06970384250176 | LD533 |
06970384250961 | LD-579 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SCIAN 88586262 not registered Live/Pending |
HONSUN (NANTONG) CO., LTD. 2019-08-20 |
SCIAN 79102301 4219933 Dead/Cancelled |
HONSUN (NANTONG) CO., LTD. 2011-08-26 |