Primary Device ID | E3120053FG12101 |
NIH Device Record Key | c62e619f-1f68-4e4f-8cee-e6b0f5d82cc6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EDENTA |
Version Model Number | 0053FG-12 |
Company DUNS | 448002915 |
Company Name | EDENTA ETABLISSEMENT |
Device Count | 12 |
DM Exempt | true |
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 | 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 |
---|---|
HIBCC | E3120053FG121 [Primary] |
HIBCC | E3120053FG12101 [Unit of Use] |
EJQ | WHEEL, POLISHING AGENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[E3120053FG12101]
Moist Heat or Steam Sterilization
[E3120053FG12101]
Moist Heat or Steam Sterilization
[E3120053FG12101]
Moist Heat or Steam Sterilization
[E3120053FG12101]
Moist Heat or Steam Sterilization
[E3120053FG12101]
Moist Heat or Steam Sterilization
[E3120053FG12101]
Moist Heat or Steam Sterilization
[E3120053FG12101]
Moist Heat or Steam Sterilization
[E3120053FG12101]
Moist Heat or Steam Sterilization
[E3120053FG12101]
Moist Heat or Steam Sterilization
[E3120053FG12101]
Moist Heat or Steam Sterilization
[E3120053FG12101]
Moist Heat or Steam Sterilization
[E3120053FG12101]
Moist Heat or Steam Sterilization
[E3120053FG12101]
Moist Heat or Steam Sterilization
[E3120053FG12101]
Moist Heat or Steam Sterilization
[E3120053FG12101]
Moist Heat or Steam Sterilization
[E3120053FG12101]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-02-11 |
Device Publish Date | 2022-02-03 |