Primary Device ID | 30850023727009 |
NIH Device Record Key | 5b767b7f-166d-41b3-8fb9-c7796f7effad |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RENPHO Pulse Oximeter |
Version Model Number | RP-PO001 |
Catalog Number | OCH |
Company DUNS | 081060692 |
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 | false |
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 | true |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com | |
Phone | 18444170149 |
support@renpho.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850023727008 [Primary] |
GS1 | 30850023727009 [Package] Contains: 00850023727008 Package: Carton [100 Units] In Commercial Distribution |
OCH | Oximeter, Infrared, Sporting, Aviation |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-23 |
Device Publish Date | 2020-09-15 |
00860002249636 | RP-PO001 |
30850023727009 | RP-PO001 |
50860002249655 | R-J002 |