Primary Device ID | 10841307112648 |
NIH Device Record Key | 659d0273-da46-45c2-8e63-6767d4eaa3d9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | simplyCrown&Bridge Legacy™ Narrow |
Version Model Number | 8757-21N |
Catalog Number | 8757-21N |
Company DUNS | 868856969 |
Company Name | IMPLANT DIRECT SYBRON MANUFACTURING LLC |
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 | true |
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 | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10841307112648 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10841307112648]
Moist Heat or Steam Sterilization
[10841307112648]
Moist Heat or Steam Sterilization
[10841307112648]
Moist Heat or Steam Sterilization
[10841307112648]
Moist Heat or Steam Sterilization
[10841307112648]
Moist Heat or Steam Sterilization
[10841307112648]
Moist Heat or Steam Sterilization
[10841307112648]
Moist Heat or Steam Sterilization
[10841307112648]
Moist Heat or Steam Sterilization
[10841307112648]
Moist Heat or Steam Sterilization
[10841307112648]
Moist Heat or Steam Sterilization
[10841307112648]
Moist Heat or Steam Sterilization
[10841307112648]
Moist Heat or Steam Sterilization
[10841307112648]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2015-09-14 |
10841307112662 | 8757-23N |
10841307112655 | 8757-22N |
10841307112648 | 8757-21N |
10841307112631 | 8745-23N |
10841307112624 | 8745-22N |
10841307112617 | 8745-21N |
10841307112600 | 8735-23N |
10841307112594 | 8735-22N |
10841307112587 | 8735-21N |