Primary Device ID | 10841307112563 |
NIH Device Record Key | d0879b82-fcc1-4204-ad35-cde345e433c8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | simplyCrown&Bridge Legacy™ |
Version Model Number | 8757-22 |
Catalog Number | 8757-22 |
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 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10841307112563 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10841307112563]
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 |
10841307112570 | 8757-23 |
10841307112563 | 8757-22 |
10841307112556 | 8757-21 |
10841307112549 | 8745-23 |
10841307112532 | 8745-22 |
10841307112525 | 8745-21 |
10841307112518 | 8735-23 |
10841307112501 | 8735-22 |
10841307112495 | 8735-21 |
10841307112488 | 8730-23 |
10841307112471 | 8730-22 |
10841307112464 | 8730-21 |