Primary Device ID | 00810125998621 |
NIH Device Record Key | 9b660c53-f0ce-48ac-9f81-1f38a7dc367f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EK Fixture Pick up Guide pin |
Version Model Number | EKPGP150 |
Company DUNS | 796083090 |
Company Name | HIOSSEN, INC. |
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 | 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 |