Primary Device ID | 16926338766665 |
NIH Device Record Key | 2ee399e5-dc5c-4ce2-bd95-35cefe9f3427 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Parent’s choice |
Version Model Number | NP-SO130F |
Company DUNS | 530853944 |
Company Name | Shanghai Foliage Industry 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 | 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 |