Primary Device ID | 00810092935209 |
NIH Device Record Key | e2052c47-f2f5-434e-8321-da833a380979 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NuSmile ZR Anterior Try-In Crown |
Version Model Number | C0R304 |
Company DUNS | 185497372 |
Company Name | NUSMILE, LTD. |
Device Count | 1 |
DM Exempt | false |
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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810092935209 [Primary] |
ELZ | Crown, Preformed |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-09-27 |
Device Publish Date | 2021-09-17 |
00810092935018 | NuSmile ZR Anterior Try-In Crown |
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