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 |