Primary Device ID | 07630031708779 |
NIH Device Record Key | 3afa29ce-06b0-459d-b4d8-f55dfb628acf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | STRAUMANN P.004 RC GOLD ABUTMENT |
Version Model Number | Final Abutments |
Catalog Number | 022.4410 |
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 | 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 | +1(800)448-8168 |
info.usa@straumann.com |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07630031708779 [Primary] |
NHA | ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07630031708779]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2015-09-24 |
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