Primary Device ID | 00841359050069 |
NIH Device Record Key | 8d6221b4-5e59-4ab3-ba92-5e044389bb9c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SABLE - Kavo Multiflex |
Version Model Number | 2000116 |
Company DUNS | 255407272 |
Company Name | Sable Industries Inc |
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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
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 | 1-800-368-8106 |
info@sableindustriesinc.com | |
Phone | 1-800-368-8106 |
info@sableindustriesinc.com | |
Phone | 1-800-368-8106 |
info@sableindustriesinc.com | |
Phone | 1-800-368-8106 |
info@sableindustriesinc.com | |
Phone | 1-800-368-8106 |
info@sableindustriesinc.com | |
Phone | 1-800-368-8106 |
info@sableindustriesinc.com | |
Phone | 1-800-368-8106 |
info@sableindustriesinc.com | |
Phone | 1-800-368-8106 |
info@sableindustriesinc.com | |
Phone | 1-800-368-8106 |
info@sableindustriesinc.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841359050069 [Primary] |
EFB | Handpiece, Air-Powered, Dental |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-08-02 |
Device Publish Date | 2022-07-25 |
00841359050076 | SABLE - KAVO Multiflex Lux Type 6-Hole Coupler w/H2O Regulator LED Engraved |
00841359050069 | SABLE - KAVO Multiflex Lux Type 6-Hole Coupler w/H2O Regulator |
00841359050052 | SABLE - KAVO Multiflex Type 5-Hole Coupler |
00841359050045 | SABLE - KAVO Multiflex Type 4-Hole Coupler w/H2O Regulator |