Primary Device ID | 00842430113420 |
NIH Device Record Key | d53fb6fd-6e56-47b0-a7d2-d4aa740a63e7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KIT, REPAIR |
Version Model Number | 10910 |
Catalog Number | 10910 |
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 | |
Phone | 1-800-777-4674 |
CustServ@mizuhosi.com | |
Phone | 1-800-777-4674 |
CustServ@mizuhosi.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00842430113420 [Primary] |
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 | 2020-08-04 |
Device Publish Date | 2020-07-27 |