Primary Device ID | 08800118611257 |
NIH Device Record Key | 294ff3d7-939b-4bd8-9ec4-5fff8d3e7589 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Everest |
Version Model Number | W MO A1 20 |
Company DUNS | 694821663 |
Company Name | U&C International Co.,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 | 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 | 08800118611257 [Primary] |
EIH | Powder, Porcelain |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-02-24 |
Device Publish Date | 2022-02-16 |