Primary Device ID | 04260242060132 |
NIH Device Record Key | 78de560d-d9d8-49f1-9621-d0a4c18aedba |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DIERS pedogait |
Version Model Number | n/a |
Company DUNS | 499189983 |
Company Name | DIERS International GmbH |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
Manufacturing Date | true |
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 | 04260242060132 [Primary] |
KHX | Platform, Force-Measuring |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-12 |
Device Publish Date | 2023-06-02 |
04260242060019 - DIERS formetric | 2023-06-12 |
04260242060064 - DIERS leg axis | 2023-06-12 |
04260242060071 - DIERS pedoscan | 2023-06-12 |
04260242060101 - DIERS statico | 2023-06-12 |
04260242060118 - DIERS myoline | 2023-06-12 |
04260242060125 - DIERS leg axis lateral | 2023-06-12 |
04260242060132 - DIERS pedogait | 2023-06-12 |
04260242060132 - DIERS pedogait | 2023-06-12 |
04260242060163 - DIERS leg axis | 2023-06-12 |