| Primary Device ID | D7701253963 |
| NIH Device Record Key | b030bb4e-79ef-489d-9e6c-b89cb40c67e6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MILLABLE REP. POST FOR |
| Version Model Number | AS-MFS-500 |
| Catalog Number | AS-MFS-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 | D7701253963 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[D7701253963]
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 | 2018-02-15 |
| D7701253963 | MILLABLE REP. POST FOR SIMPLE TECH,D.5.00 MM EX.2.30 |
| D7701245763 | MILLABLE REP. POST FOR SIMPLE TECH,D.4.25 MM EX.2.30 |
| D7700877413 | MILLABLE REP. POST FOR INTERCEPT. TECH.,PRE-KOH 5.00 |
| D7700877403 | MILLABLE REP. POST FOR INTERCEPT. TECH.,PRE-KOH 4.25 |
| D7700877393 | MILLABLE REP. POST FOR INTERCEPT. TECH.,PRE-KOH 3.80 |
| D7700635853 | MILLABLE REP. POST FOR SIMPLE TECHNIQUE, PRE-KOH 5.00 |
| D7700635843 | MILLABLE REP. POST FOR SIMPLE TECHNIQUE, PRE-KOH 4.25 |
| D7700635833 | MILLABLE REP. POST FOR SIMPLE TECHNIQUE, PRE-KOH 3.80 |
| D7700635823 | MILLABLE REP. POST FOR SIMPLE TECHNIQUE, PREMIUM 3.30 |