Primary Device ID | 10842430105835 |
NIH Device Record Key | 1fdda2a0-d0c1-4070-8912-296b7dae194b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CONVOLUTED FOAM PAD |
Version Model Number | 1901 |
Catalog Number | 1901-12 |
Company DUNS | 084527241 |
Company Name | MIZUHO ORTHOPEDIC SYSTEMS, INC. |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 1-800-777-4674 |
CustServ@mizuhosi.com | |
Phone | 1-800-777-4674 |
CustServ@mizuhosi.com | |
Phone | 1-800-777-4674 |
CustServ@mizuhosi.com | |
Phone | 1-800-777-4674 |
CustServ@mizuhosi.com | |
Phone | 1-800-777-4674 |
CustServ@mizuhosi.com | |
Phone | 1-800-777-4674 |
CustServ@mizuhosi.com | |
Phone | 1-800-777-4674 |
CustServ@mizuhosi.com | |
Phone | 1-800-777-4674 |
CustServ@mizuhosi.com | |
Phone | 1-800-777-4674 |
CustServ@mizuhosi.com | |
Phone | 1-800-777-4674 |
CustServ@mizuhosi.com | |
Phone | 1-800-777-4674 |
CustServ@mizuhosi.com | |
Phone | 1-800-777-4674 |
CustServ@mizuhosi.com | |
Phone | 1-800-777-4674 |
CustServ@mizuhosi.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00842430105838 [Primary] |
GS1 | 10842430105835 [Package] Contains: 00842430105838 Package: CASE [12 Units] In Commercial Distribution |
FMP | Protector, Skin Pressure |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-01-29 |
Device Publish Date | 2020-01-21 |