Primary Device ID | 10810140060669 |
NIH Device Record Key | b06d5874-6f11-4fc0-aa4f-6b1c170945e1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RENPHO Smart scale |
Version Model Number | R-A016 |
Company DUNS | 033774836 |
Company Name | Joicom Corporation |
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 | 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 | 00810140060662 [Primary] |
GS1 | 10810140060669 [Package] Contains: 00810140060662 Package: case [5 Units] In Commercial Distribution |
PUH | Analyzer, Body Composition, Exempt |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-15 |
Device Publish Date | 2023-08-07 |
10810140060744 | R-A020 |
10810140060737 | R-A020 |
10810140060720 | R-A011 |
10810140060690 | R-A016 |
10810140060669 | R-A016 |
10810140060652 | R-A001 |
10810140060638 | R-A005 |
10810140060621 | ES-BR001 |
10810140060553 | R-A002 |
10810140060096 | ES-WBE28 |
10810140060072 | R-A012 |