Micro-Stix
GUDID 20789594000842
YOUNG MICROBRUSH, LLC
General-purpose absorbent tip applicator/swab, single-use| Primary Device ID | 20789594000842 |
| NIH Device Record Key | 56a63eba-781d-442e-819b-d34c907506d4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Micro-Stix |
| Version Model Number | -STIX64B |
| Company DUNS | 929236305 |
| Company Name | YOUNG MICROBRUSH, 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 | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00789594000848 [Primary] |
| GS1 | 10789594000845 [Package] Contains: 00789594000848 Package: [64 Units] In Commercial Distribution |
| GS1 | 20789594000842 [Package] Contains: 10789594000845 Package: [24 Units] In Commercial Distribution |
FDA Product Code
| EJB | HANDLE, INSTRUMENT, DENTAL |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-12-16 |
| Device Publish Date | 2020-12-08 |
On-Brand Devices [Micro-Stix]
| 20789594000989 | 291784 |
| 20789594000842 | -STIX64B |
Trademark Results [Micro-Stix]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MICRO-STIX 86593117 4907486 Live/Registered |
Young Microbrush, LLC 2015-04-10 |
 MICRO-STIX 77302203 3607837 Live/Registered |
Young Microbrush, LLC 2007-10-11 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.