| Primary Device ID | 06933192201112 |
| NIH Device Record Key | ae7c1994-223e-4da7-a25b-68a95ca5df45 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Hakuna Matata |
| Version Model Number | WGBZ01-50 |
| Company DUNS | 526901386 |
| Company Name | FUJIAN BBC INC |
| 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 | false |
| Serial Number | false |
| Manufacturing Date | true |
| 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 | 06933192201112 [Primary] |
| KHA | Mask, Scavenging |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-12-15 |
| Device Publish Date | 2022-12-07 |