Primary Device ID | 00842271103475 |
NIH Device Record Key | a115ed16-48c7-4ddc-9cc4-ffcc57b5eae2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NexxZr™ T / W-98-20-NT-A200-SD |
Version Model Number | W-32017 |
Company DUNS | 002265727 |
Company Name | SAGEMAX BIOCERAMICS, 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 | 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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00842271103475 [Primary] |
EIH | Powder, Porcelain |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-07-24 |
Device Publish Date | 2018-03-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NEXXZR 85234108 4136586 Live/Registered |
Sagemax Bioceramics, Inc. 2011-02-04 |