Primary Device ID | 50732224002939 |
NIH Device Record Key | 03d50d0e-210a-4588-971c-19a8d54e7fbe |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sparkle™ Prophy Angle |
Version Model Number | TPATBC1 |
Company DUNS | 057728685 |
Company Name | CROSSTEX INTERNATIONAL, INC. |
Device Count | 100 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00732224002934 [Unit of Use] |
GS1 | 10732224002931 [Primary] |
GS1 | 50732224002939 [Package] Contains: 10732224002931 Package: [4 Units] In Commercial Distribution |
EFA | Handpiece, belt and/or gear driven, dental |
EGS | Handpiece, contra- and right-angle attachment, 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 | 2022-10-07 |
Device Publish Date | 2022-09-29 |
50732224002953 | Prophy Angles, Soft Cup, Purple |
50732224002946 | Prophy Angles, Disposable, Firm Cup White |
50732224002939 | Prophy Angle,Tapered Brush |
50732224002922 | Prophy Angles, Soft Cup, Purple |
50732224002915 | Prophy Angle, Firm Cup, White |