Primary Device ID | 00842271105288 |
NIH Device Record Key | 3161f7dd-3911-46da-8f2e-d6342c8e79d4 |
Commercial Distribution Discontinuation | 2018-04-16 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | NexxZr™ T / W-98-35-NT-OM20-SD |
Version Model Number | W-32198 |
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 | 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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00842271105288 [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 |