Primary Device ID | 00697038425648 |
NIH Device Record Key | 5603f0a1-26da-4c4f-847e-f02cab5f4be7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dittmann |
Version Model Number | LD-753 |
Company DUNS | 543364560 |
Company Name | HONSUN (NANTONG) CO.,LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
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 | 00697038425648 [Primary] |
DXN | System, Measurement, Blood-Pressure, Non-Invasive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2018-02-03 |
16970384254515 - / | 2024-09-17 |
06970384250800 - Take a breath | 2022-04-08 |
06970384250961 - SCIAN | 2022-04-08 |
06970384250176 - SCIAN | 2022-04-08 |
06970384250183 - SCIAN | 2022-04-08 |
06970384250213 - SCIAN | 2022-04-08 |
06970384250220 - HONSUN | 2022-04-08 |
06970384250435 - SCIAN | 2022-04-08 |