Primary Device ID | D7701306503 |
NIH Device Record Key | a48afbc6-0828-4d38-8a3b-e0e881efc919 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ANGLED PRE-MADE ABUTMENT |
Version Model Number | A-MA05-TS-EX230 |
Catalog Number | A-MA05-TS-EX230 |
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 | D7701306503 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[D7701306503]
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 | 2017-03-28 |
D7701306503 | ANGLED PRE-MADE ABUTMENT 5GR, HEX 2,30 MM, PRE-KOH |
D7701096153 | ANGLED PRE-MADE ABUTMENT 15GR, HEX 2,50 MM, PRE-KOH |
D7701096143 | ANGLED PRE-MADE ABUTMENT 10GR, HEX 2,50 MM, PRE-KOH |
D7701096133 | ANGLED PRE-MADE ABUTMENT 5GR, HEX 2,50 MM, PRE-KOH |
D7701096123 | ANGLED PRE-MADE ABUTMENT 15GR, HEX 2,30 MM, PRE-KOH |
D7701096113 | ANGLED PRE-MADE ABUTMENT 10GR, HEX 2,30 MM, PRE-KOH |
D7701441233 | ANGLED PRE-MADE ABUTMENT 15GR, D.3.80 MM, H. 2 |
D7701441223 | ANGLED PRE-MADE ABUTMENT 7.5GR, D.3.80 MM, H. 2 |
D7701441203 | ANGLED PRE-MADE ABUTMENT 15GR, D.3.30 MM, H. 2 |
D7701441193 | ANGLED PRE-MADE ABUTMENT 7.5GR, D.3.30 MM, H. 2 |