Primary Device ID | 00852673007066 |
NIH Device Record Key | c51dc8c1-db16-49de-a71c-2a45e013949c |
Commercial Distribution Discontinuation | 2018-12-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Propel |
Version Model Number | ASM-20022 |
Catalog Number | ASM-20022 |
Company DUNS | 117334253 |
Company Name | PROPEL ORTHODONTICS LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
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 | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com | |
Phone | 408 394 5851 |
bw@propelortho.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00852673007066 [Primary] |
ECR | Setter, Band, Orthodontic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-01-23 |
Device Publish Date | 2018-03-06 |
00852673007097 | VPro+ |
00852673007080 | C-Shaped Vibration Device, Brazil |
00852673007073 | Packaged C-Shaped Mouthpiece, Tapered, Assy |
00852673007066 | Packaged Mouthpiece, Single, Assy |
00852673007059 | Assy. Packaged Disposable Drill Tip-Open |
00852673007042 | Propel, Reusable Handle |
00852673007035 | Assy. Packaged Disposable Drill Tip, Closed |
00852673007028 | Assy. Packaged Perforation Device, Contra-Angle |
00852673007011 | C-Shaped Vibration Device |
00852673007004 | Perforation Device, Propel XL |