Primary Device ID | 04548190201334 |
NIH Device Record Key | aaf8a0c4-638a-4b37-9677-a07ceabbe8b1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tokuso Rebase MR Bond |
Version Model Number | 20133 |
Company DUNS | 693552176 |
Company Name | TOKUYAMA DENTAL CORPORATION |
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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1-877-378-3548 |
info@tokuyama-us.com |
Storage Environment Temperature | Between 0 Degrees Celsius and 10 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04548190201334 [Primary] |
KLE | Agent, Tooth Bonding, Resin |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-08-09 |
Device Publish Date | 2016-09-23 |
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