Primary Device ID | D7700633963 |
NIH Device Record Key | 95c3f4e2-9e94-4593-81c4-8f07c79b26a8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CASTABLE REP. POST WITH GOLD |
Version Model Number | A-UCR-425-EX |
Catalog Number | A-UCR-425-EX |
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 | D7700633963 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[D7700633963]
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 |
D7701253983 | CASTABLE REP. POST WITH GOLD BASE,D.5.00 MM EX.2.30 |
D7701245783 | CASTABLE REP. POST WITH GOLD BASE,D.4.25 MM EX.2.30 |
D7700884233 | CASTABLE REP. POST WITH GOLD BASE, PRE-KOH TG,WIDE PLATFORM |
D7700884223 | CASTABLE REP. POST WITH GOLD BASE, PRE-KOH TG, MEDIUM PLAT. |
D7700884193 | CASTABLE REP. POST WITH GOLD BASE, PRE-KOH TG, WIDE PLAT. |
D7700884183 | CASTABLE REP. POST WITH GOLD BASE, PRE-KOH TG, MEDIUM PLAT. |
D7700633983 | CASTABLE REP. POST WITH GOLD BASE, PREMIUM D.3.30 MM |
D7700633973 | CASTABLE REP. POST WITH GOLD BASE, PRE-KOH D.3.80 MM |
D7700633963 | CASTABLE REP. POST WITH GOLD BASE, PRE-KOH D.4.25 MM |
D7700633953 | CASTABLE REP. POST WITH GOLD BASE, PRE-KOH D.5.00 MM |