Primary Device ID | 00812926020228 |
NIH Device Record Key | c4b7c7ba-67c9-4efa-8ebc-07e2bf8876cd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 3S Hemi Impactor |
Version Model Number | 111-00-012 |
Company DUNS | 828829072 |
Company Name | TRILLIANT SURGICAL, LTD. |
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 | 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 | 00812926020228 [Primary] |
HWA | Impactor |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
[00812926020228]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-24 |
Device Publish Date | 2018-09-23 |