STRAUMANN CARES BONE LEVEL SCREW RETAINED BARS, STRAUMANN CARES BONE LEVEL SCREW 010.1151

GUDID 07630031702814

CARES® Milled Bar, 4 Implants, Ti/TAN

Institut Straumann AG

Dental bridge, metal-ceramic Dental bridge, metal-ceramic Dental bridge, metal-ceramic Dental bridge, metal-ceramic Dental bridge, metal-ceramic Dental bridge, metal-ceramic Dental bridge, metal-ceramic Dental bridge, metal-ceramic Dental bridge, metal-ceramic Dental bridge, metal-ceramic Dental bridge, metal-ceramic Dental bridge, metal-ceramic Dental bridge, metal-ceramic Dental bridge, metal-ceramic Dental bridge, metal-ceramic Dental bridge, metal-ceramic Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed
Primary Device ID07630031702814
NIH Device Record Key9a5ae2f6-57b8-4253-b6fd-2f3c96335360
Commercial Distribution StatusIn Commercial Distribution
Brand NameSTRAUMANN CARES BONE LEVEL SCREW RETAINED BARS, STRAUMANN CARES BONE LEVEL SCREW
Version Model NumberBridges (implant borne)
Catalog Number010.1151
Company DUNS483599259
Company NameInstitut Straumann AG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com
Phone+1(800)448-8168
Emailinfo.usa@straumann.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107630031702814 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


[07630031702814]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-04-04
Device Publish Date2016-10-20

Devices Manufactured by Institut Straumann AG

07630031775580 - Straumann® Variobase® Abutments and Straumann® n!ce® Zirconia discs2024-04-25 n!ce ZirconiaHT, Multi BL3, 14mm
07630031775597 - Straumann® Variobase® Abutments and Straumann® n!ce® Zirconia discs2024-04-25 n!ce ZirconiaHT, Multi BL3, 16mm
07630031775603 - Straumann® Variobase® Abutments and Straumann® n!ce® Zirconia discs2024-04-25 n!ce ZirconiaHT, Multi BL3, 20mm
07630031775610 - Straumann® Variobase® Abutments and Straumann® n!ce® Zirconia discs2024-04-25 n!ce ZirconiaHT, Multi BL3, 25mm
07630031775627 - Straumann® Variobase® Abutments and Straumann® n!ce® Zirconia discs2024-04-25 n!ce ZirconiaHT, Multi BL3, 30mm
07630031771452 - Straumann Variobase C2024-04-11 RB/WB Variobase C, incl. screw, Ø 4.5mm, GH 2.5mm, TAN
07630031771469 - Straumann Variobase C2024-04-11 RB/WB Variobase C, incl. screw, Ø 4.5mm, GH 3.5mm, TAN
07630031771476 - Straumann Variobase C2024-04-11 WB Variobase C, incl. screw, Ø 5.5mm, GH 0.75mm, TAN

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