Primary Device ID | 07332747004366 |
NIH Device Record Key | 8e1d1030-98a4-4182-8ea6-057dfb22cf46 |
Commercial Distribution Discontinuation | 2018-03-14 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | 32349 |
Catalog Number | 32349 |
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 | 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 | true |
OTC Over-The-Counter | false |
Phone | +1(800)322-5001 |
us.customerservice@nobelbiocare.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07332747004366 [Primary] |
DZE | IMPLANT, ENDOSSEOUS, ROOT-FORM |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2015-09-17 |
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07332747207835 - NA | 2025-05-26 Implant Analog 5.0 HL/RPL |
07332747207880 - NA | 2025-05-26 Implant Analog 6.0 HL/RPL |
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07332747207910 - NA | 2025-05-26 Replica Fixture Novum |
07332747207927 - Brånemark System® | 2025-05-26 Screw Ceramic Abutment Bmk Syst RP |