Primary Device ID | 08809917144584 |
NIH Device Record Key | 0d28436a-315e-4c5f-a899-d58a5030e606 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HySil Plus Impression Materials |
Version Model Number | ESS50LSB |
Company DUNS | 694893867 |
Company Name | Osstem Implant 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 | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08809917144584 [Primary] |
ELW | Material, Impression |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-11-22 |
Device Publish Date | 2023-11-14 |
08800121709309 | ESS50MSB |
08800121709293 | ESS50HSB |
08800121709286 | ESS50LSB |
08800121709279 | ESS50LSD |
08800121709262 | ESS50LS |
08800121709255 | ESS50HS |
08800121709248 | ESS380HS |
08800121709231 | ESS50MS |
08800121709224 | ESS50MSD |
08800121709217 | ESS50HSD |
08809917144638 | ESS50HS |
08809917144621 | ESS50HSD |
08809917144614 | ESS50HSB |
08809917144607 | ESS50LS |
08809917144591 | ESS50LSD |
08809917144584 | ESS50LSB |
08809917144577 | ESS50MS |
08809917144560 | ESS50MSD |
08809917144553 | ESS50MSB |
08800121773621 | ESS380MS |