Primary Device ID | 06971519616584 |
NIH Device Record Key | e1cf5a5f-bb6a-4d1d-8278-3c3a10980d8c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HF |
Version Model Number | HFFAB1-2 |
Company DUNS | 529497551 |
Company Name | Anji Hengfeng Sanitary Material 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 | true |
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 |