Primary Device ID | 00842430100079 |
NIH Device Record Key | aa5787c2-6ba6-4aa4-ba96-3ac9a6b5c5d2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Restraint Straps |
Version Model Number | 9600-787 |
Catalog Number | 9600-787 |
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 | false |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00842430100079 [Primary] |
FMQ | Restraint, Protective |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-02-21 |
Device Publish Date | 2018-05-23 |