Gingiva former (4-lobe), PF 4.5, H 5.7 mm
GUDID 07640182642051
Thommen Medical AG
Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Primary Device ID | 07640182642051 |
NIH Device Record Key | b53124e9-e587-4452-8c38-d6be4dfbbd29 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Gingiva former (4-lobe), PF 4.5, H 5.7 mm |
Version Model Number | 4.03.561 |
Company DUNS | 481614829 |
Company Name | Thommen Medical 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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Identifiers
Device Issuing Agency | Device ID |
---|
GS1 | 07640182642051 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
FDA Product Code
NHA | Abutment, Implant, Dental, Endosseous |
Sterilization
Steralize Prior To Use | true |
Device Is Sterile | false |
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
[07640182642051]
Moist Heat or Steam Sterilization
Device Entry Metadata
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-01 |
Device Publish Date | 2023-05-24 |
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