Primary Device ID | 07290015358910 |
NIH Device Record Key | 94afda04-844a-4fa9-beae-ddca3109b053 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ProGlass Two |
Version Model Number | 172002-A2 |
Catalog Number | 172002-A2 |
Company DUNS | 600071344 |
Company Name | SILMET 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 | false |
Expiration Date | true |
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 |
---|---|
GS1 | 07290015358910 [Primary] |
EMA | Cement, Dental |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-12-03 |
Device Publish Date | 2016-11-28 |
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07290015358910 | Dental Glass Ionomer Cement |
07290015358903 | Dental Glass Ionomer Cement |