| Primary Device ID | 06976057000017 |
| NIH Device Record Key | 9573e1bc-e455-4a06-9a83-001d790130e8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CHENGFENG |
| Version Model Number | CF-1 |
| Company DUNS | 420754459 |
| Company Name | Dongguan Chengfeng Industrial Co., Ltd. |
| 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 | true |
| Manufacturing Date | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06976057000017 [Primary] |
| FMR | Device, Transfer, Patient, Manual |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-04-26 |
| Device Publish Date | 2023-04-18 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CHENGFENG 90400019 not registered Live/Pending |
Guangzhou Chengfeng Xiongdi Industrial Co., Ltd. 2020-12-21 |
![]() CHENGFENG 88557404 not registered Live/Pending |
Guangzhou Chengfeng Brother Industrial Co., Ltd. 2019-08-01 |