Primary Device ID | 00814356025811 |
NIH Device Record Key | 743af3e7-3ae6-43f5-8049-88fee959d6b6 |
Commercial Distribution Discontinuation | 2018-08-06 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | NexxZr™ Plus / A-71-30-NP-C300-SD |
Version Model Number | A-22131 |
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 | 00814356025811 [Primary] |
EIH | Powder, Porcelain |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-08-07 |
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 |