| Primary Device ID | 07332747000818 |
| NIH Device Record Key | 42af0a4b-c65d-451f-83e5-128928044f87 |
| Commercial Distribution Discontinuation | 2018-03-14 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | 29476 |
| Catalog Number | 29476 |
| 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 | false |
| 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 | 07332747000818 [Primary] |
| DZE | IMPLANT, ENDOSSEOUS, ROOT-FORM |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07332747000818]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2015-09-17 |
| 07332747225549 - NobelActive® | 2026-03-10 Guided Implant Mount NobelActive S 4.3 |
| 07332747225556 - NobelActive® | 2026-03-10 Guided Implant Mount NobelActive S 5.0 |
| 07332747225563 - NA | 2026-03-10 Guided Implant Mount CC S 4.3 |
| 07332747225570 - NA | 2026-03-10 Guided Implant Mount CC S 5.0/5.5 |
| 07332747225587 - NA | 2026-03-10 Guided Templ Abutm w Screw CC S 4.3 |
| 07332747225594 - NA | 2026-03-10 Guided Templ Abutm w Screw CC S 5.0/5.5 |
| 07332747225839 - NobelActive® | 2026-03-10 Guided Implant Mount NobelActive S 5.5 |
| 07332747221947 - NobelActive® S TiUltra™ | 2026-03-06 NobelActive® S TiUltra™ NP 3.5x8.5mm |