Primary Device ID | 07332747106268 |
NIH Device Record Key | 1358b5d3-ccfc-44b9-876d-999d05cf16a7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NobelDesign™ |
Version Model Number | 1.1 |
Catalog Number | 38412 |
Company DUNS | 353939929 |
Company Name | Nobel Biocare AB |
Device Count | 1 |
DM Exempt | true |
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 | 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 | 07332747106268 [Primary] |
NHA | ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-05-31 |
Device Publish Date | 2016-09-17 |
07332747125191 | NobelDesign 1.4 for Windows 64-bit |
07332747124736 | NobelDesign 1.3 for Windows 64-bit |
07332747106268 | NobelDesign 1.1 for Windows 64-bit |