Primary Device ID | 05060440330742 |
NIH Device Record Key | 002737b0-644e-4b38-a582-0e1e5ebce4f5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Neoss Implant System |
Version Model Number | 31285 |
Catalog Number | 31285 |
Company DUNS | 216693627 |
Company Name | Neoss Ltd |
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 | false |
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 | 05060440330742 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[05060440330742]
Moist Heat or Steam Sterilization
[05060440330742]
Moist Heat or Steam Sterilization
[05060440330742]
Moist Heat or Steam Sterilization
[05060440330742]
Moist Heat or Steam Sterilization
[05060440330742]
Moist Heat or Steam Sterilization
[05060440330742]
Moist Heat or Steam Sterilization
[05060440330742]
Moist Heat or Steam Sterilization
[05060440330742]
Moist Heat or Steam Sterilization
[05060440330742]
Moist Heat or Steam Sterilization
[05060440330742]
Moist Heat or Steam Sterilization
[05060440330742]
Moist Heat or Steam Sterilization
[05060440330742]
Moist Heat or Steam Sterilization
[05060440330742]
Moist Heat or Steam Sterilization
[05060440330742]
Moist Heat or Steam Sterilization
[05060440330742]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-05-26 |
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