Primary Device ID | 10841307124825 |
NIH Device Record Key | 098632ef-c2b6-4191-b54b-9e45558905a9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DLC Step Drill 4.8/4.4mm (6-13mmL) |
Version Model Number | SD4.8CS |
Catalog Number | SD4.8CS |
Company DUNS | 868856969 |
Company Name | IMPLANT DIRECT SYBRON MANUFACTURING LLC |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
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 | |
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 Issuing Agency | Device ID |
---|---|
GS1 | 10841307124825 [Primary] |
DZI | Drill, Bone, Powered |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10841307124825]
Moist Heat or Steam Sterilization
[10841307124825]
Moist Heat or Steam Sterilization
[10841307124825]
Moist Heat or Steam Sterilization
[10841307124825]
Moist Heat or Steam Sterilization
[10841307124825]
Moist Heat or Steam Sterilization
[10841307124825]
Moist Heat or Steam Sterilization
[10841307124825]
Moist Heat or Steam Sterilization
[10841307124825]
Moist Heat or Steam Sterilization
[10841307124825]
Moist Heat or Steam Sterilization
[10841307124825]
Moist Heat or Steam Sterilization
[10841307124825]
Moist Heat or Steam Sterilization
[10841307124825]
Moist Heat or Steam Sterilization
[10841307124825]
Moist Heat or Steam Sterilization
[10841307124825]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-08-18 |
Device Publish Date | 2020-08-10 |