Primary Device ID | 07630031710529 |
NIH Device Record Key | 4995a3db-e3aa-4846-8fe8-bc61221c9c18 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | STRAUMANN DENTAL IMPLANT SYSTEM |
Version Model Number | 1 |
Catalog Number | 024.4105-04 |
Company DUNS | 483599259 |
Company Name | Institut Straumann AG |
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 | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com | |
Phone | +1(800)448-8168 |
info.usa@straumann.com |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Length | 0.5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07630031710529 [Primary] |
DZE | IMPLANT, ENDOSSEOUS, ROOT-FORM |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
[07630031710529]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-12-07 |
Device Publish Date | 2015-09-24 |
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