Primary Device ID | 00810140061492 |
NIH Device Record Key | 964e4077-5353-4720-867f-d6ee5183d21f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RENPHO Eye Massager |
Version Model Number | R-GC001 |
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 | 00810140061492 [Primary] |
GS1 | 10810140061499 [Package] Package: case [24 Units] In Commercial Distribution |
ISA | Massager, Therapeutic, Electric |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-06-06 |
Device Publish Date | 2025-05-29 |
10810140061185 | R-G010V |
10810140060492 | R-G006 |
10810140060485 | R-G006 |
10810140060478 | R-G006 |
10810140060461 | R-G004 |
10810140060447 | RF-EM001R |
10810140060430 | RF-EM001R |
10810140060393 | RF-EM001 |
10810140060386 | RF-EM001 |
10810140060379 | RF-EM001 |
00810140062499 | R-WME02 |
00810140062451 | R-G006 |
00810140062444 | R-WME04 |
00810140062437 | R-WME02 |
00810140061928 | RF-EM001V |
00810140061911 | R-G010V |
00810140061775 | R-WME01 |
00810140061713 | R-G010V |
00810140061584 | R-G011 |
00810140061577 | RF-EM001V |
00810140061508 | R-G006 |
00810140061492 | R-GC001 |
00810140061485 | R-G010V |
00810140061263 | RF-EM001 |
00810140061249 | RF-EM001 |