Noritake Super Porcelain EX-3
GUDID EKUR1022261KA0
3110B 10g
KURARAY NORITAKE DENTAL INC.
Dental appliance fabrication material, ceramic| Primary Device ID | EKUR1022261KA0 |
| NIH Device Record Key | 8b6481a3-aa83-4950-a838-77bda0340a98 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Noritake Super Porcelain EX-3 |
| Version Model Number | 102-2261KA |
| Company DUNS | 697119498 |
| Company Name | KURARAY NORITAKE DENTAL INC. |
| 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 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | EKUR1022261KA0 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K193060
FDA Product Code
| EIH | Powder, Porcelain |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-05-08 |
| Device Publish Date | 2017-02-17 |
On-Brand Devices [Noritake Super Porcelain EX-3]
Trademark Results [Noritake Super Porcelain EX-3]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NORITAKE SUPER PORCELAIN EX-3 74336446 1807301 Live/Registered |
NORITAKE CO., LIMITED 1992-12-03 |
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