Primary Device ID | D7700875033 |
NIH Device Record Key | 57c2f090-4dbf-4cd0-8cbc-3499037dff65 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CASTABLE CAP FOR PREMADE POSTS |
Version Model Number | A-TG-CAPCM-W-ROT |
Catalog Number | A-TG-CAPCM-W-ROT |
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 | D7700875033 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[D7700875033]
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 | 2015-10-01 |
D7700875033 | CASTABLE CAP FOR PREMADE POSTS NON REP., PREKOHTG, WIDE PLAT. |
D7700875023 | CASTABLE CAP FOR PREMADE POSTS NON REP.,PREKOHTG,MEDIUM PLAT. |
D7700875013 | CASTABLE CAP FOR PREMADE POSTS REP., PRE-KOH TG, WIDE PLAT. |
D7700875003 | CASTABLE CAP FOR PREMADE POSTS REP., PRE-KOH TG, MEDIUM PLAT. |