Primary Device ID | 00083208335143 |
NIH Device Record Key | ff5d3955-fd29-470d-865c-8c975baaca36 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tatum Surgical/One Piece Crown and Bridge Angled head implant |
Version Model Number | One Piece/3.5 x 14CBA |
Catalog Number | ITO3.5x14CBA |
Company DUNS | 078352849 |
Company Name | Suncoast Dental, Inc |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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(727)536-4880 |
tatumimplants@verivon.net | |
Phone | +1(727)536-4880 |
tatumcompliance@gmail.com | |
Phone | +1(727)536-4880 |
tatumcompliance@gmail.com | |
Phone | +1(727)536-4880 |
tatumcompliance@gmail.com | |
Phone | +1(727)536-4880 |
tatumcompliance@gmail.com | |
Phone | +1(727)536-4880 |
tatumcompliance@gmail.com | |
Phone | +1(727)536-4880 |
tatumcompliance@gmail.com | |
Phone | +1(727)536-4880 |
tatumcompliance@gmail.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Length | 14 Millimeter |
Outer Diameter | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 14 Millimeter |
Outer Diameter | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 14 Millimeter |
Outer Diameter | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 14 Millimeter |
Outer Diameter | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 14 Millimeter |
Outer Diameter | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 14 Millimeter |
Outer Diameter | 3.5 Millimeter |
Device Size Text, specify | 0 |
Length | 14 Millimeter |
Outer Diameter | 3.5 Millimeter |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00083208335143 [Primary] |
DZE | IMPLANT, ENDOSSEOUS, ROOT-FORM |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00083208335143]
Moist Heat or Steam Sterilization
[00083208335143]
Moist Heat or Steam Sterilization
[00083208335143]
Moist Heat or Steam Sterilization
[00083208335143]
Moist Heat or Steam Sterilization
[00083208335143]
Moist Heat or Steam Sterilization
[00083208335143]
Moist Heat or Steam Sterilization
[00083208335143]
Moist Heat or Steam Sterilization
[00083208335143]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-30 |
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