| Primary Device ID | D7701067713 |
| NIH Device Record Key | 6e4a823e-1db2-4c05-8bf9-f2866f577b44 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CAST. NON REP. POST WITH CRCO |
| Version Model Number | A-UCRCO-500 |
| Catalog Number | A-UCRCO-500 |
| Company DUNS | 433815198 |
| Company Name | SWEDEN & MARTINA SPA |
| 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 | true |
| Lot Batch | true |
| Serial Number | true |
| 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 | 844.862.7846 |
| info.us@sweden-martina.com |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | D7701067713 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[D7701067713]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2015-09-23 |
| D7701254013 | CAST. NON REP. POST WITH CRCO BASE,D.5.00 MM EX.2.30 |
| D7701245813 | CAST. NON REP. POST WITH CRCO BASE,D.4.25 MM EX.2.30 |
| D7701067713 | CAST. NON REP. POST WITH CRCO BASE, PRE-KOH D.5,00 MM |
| D7701067703 | CAST. NON REP. POST WITH CRCO BASE, PRE-KOH D.4.25 MM |
| D7701067693 | CAST. NON REP. POST WITH CRCO BASE, PRE-KOH D.3,80 MM |
| D7701067683 | CAST. NON REP. POST WITH CRCO BASE, PREMIUM D.3,30 MM |