Primary Device ID | 10841307109747 |
NIH Device Record Key | 45b5924d-dc49-4a16-8af3-a4c2a334084c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | InterActive® GPS® Abutment Narrow |
Version Model Number | 6530-94N |
Catalog Number | 6530-94N |
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 | 10841307109747 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10841307109747]
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 |
10841307109822 | 6534-96N |
10841307109815 | 6534-95N |
10841307109808 | 6534-94N |
10841307109792 | 6534-93N |
10841307109785 | 6534-92N |
10841307109778 | 6534-91N |
10841307109761 | 6530-96N |
10841307109754 | 6530-95N |
10841307109747 | 6530-94N |
10841307109730 | 6530-93N |
10841307109723 | 6530-92N |
10841307109716 | 6530-91N |