Primary Device ID | 00810140062253 |
NIH Device Record Key | 42a03fdc-5850-499e-8e4c-1a0e440c56c0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RENPHO Heating Pad |
Version Model Number | R-HAP67 |
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 | 00810140062253 [Primary] |
GS1 | 10810140062250 [Package] Package: case [16 Units] In Commercial Distribution |
IRT | Pad, Heating, Powered |
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 |
10810140061161 | R-U011 |
10810140061130 | NA-H1222D |
10810140061123 | NA-H1222D |
10810140061116 | NA-H1222D |
10810140061109 | NA-H1222D |
10810140061093 | NA-H1222D |
10810140061086 | NA-H1222D |
10810140061079 | R-U002 |
10810140061062 | R-U002 |
10810140061055 | R-U002 |
10810140061048 | R-U005 |
10810140061031 | R-U006 |
10810140061024 | R-U006 |
10810140061017 | R-U006 |
10810140061000 | R-U010 |
00810140062260 | R-HAP68 |
00810140062253 | R-HAP67 |
00810140062246 | R-HAP64 |
00810140062178 | R-HAP61 |
00810140062161 | R-HAP03 |
00810140062154 | R-HAP02 |
00810140062147 | R-HAP01 |