Primary Device ID | 10810140060997 |
NIH Device Record Key | 717c77c6-bed4-414b-890f-a39335b3c04f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RENPHO Automatic Blood Pressure Monitor |
Version Model Number | R-J004 |
Company DUNS | 033774836 |
Company Name | Joicom Corporation |
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 | 00810140060990 [Primary] |
GS1 | 10810140060997 [Package] Contains: 00810140060990 Package: case [12 Units] In Commercial Distribution |
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 | 2 |
Public Version Date | 2025-02-17 |
Device Publish Date | 2023-08-08 |
00810140061249 - RENPHO Eye Massager | 2025-06-06 |
00810140061263 - RENPHO Eye Massager | 2025-06-06 |
00810140061485 - RENPHO Eye Massager | 2025-06-06 |
00810140061492 - RENPHO Eye Massager | 2025-06-06 |
00810140061508 - RENPHO Eye Massager | 2025-06-06 |
00810140061577 - RENPHO Eye Massager | 2025-06-06 |
00810140061584 - RENPHO Eye Massager | 2025-06-06 |
00810140061713 - RENPHO Eye Massager | 2025-06-06 |