Primary Device ID | G001HSB1072000 |
NIH Device Record Key | c9eb2343-2541-448f-a6fd-c5dd350a0ef4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | House Brand |
Version Model Number | HSB-107200 |
Company DUNS | 529534554 |
Company Name | Chengdu Xinjin Shifeng Medical Apparatus & Instrument 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 |