Primary Device ID | 00873263008188 |
NIH Device Record Key | bd555fad-2e3d-4208-af8c-998e9bb3585a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Resident Expert Software Module |
Version Model Number | C0258-00818 |
Catalog Number | C0258 |
Company DUNS | 108179458 |
Company Name | FHC, INC. |
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 | 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 | true |
OTC Over-The-Counter | false |
Phone | +1(800)326-2905 |
fhcinc@fh-co.com | |
Phone | +1(800)326-2905 |
fhcinc@fh-co.com | |
Phone | +1(800)326-2905 |
fhcinc@fh-co.com | |
Phone | +1(800)326-2905 |
fhcinc@fh-co.com | |
Phone | +1(800)326-2905 |
fhcinc@fh-co.com | |
Phone | +1(800)326-2905 |
fhcinc@fh-co.com | |
Phone | +1(800)326-2905 |
fhcinc@fh-co.com | |
Phone | +1(800)326-2905 |
fhcinc@fh-co.com | |
Phone | +1(800)326-2905 |
fhcinc@fh-co.com | |
Phone | +1(800)326-2905 |
fhcinc@fh-co.com | |
Phone | +1(800)326-2905 |
fhcinc@fh-co.com | |
Phone | +1(800)326-2905 |
fhcinc@fh-co.com | |
Phone | +1(800)326-2905 |
fhcinc@fh-co.com | |
Phone | +1(800)326-2905 |
fhcinc@fh-co.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00873263008188 [Primary] |
GZL | ELECTRODE, DEPTH |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-08-18 |
Device Publish Date | 2020-08-10 |
00873263008089 | Guideline 4000™ Resident Expert Software Module, 1x |
00873263008188 | Guideline 4000™ Resident Expert Software Module, 1x |