Primary Device ID | 00616784704517 |
NIH Device Record Key | fe67ce2c-ab1d-40ba-b5fe-3582acf60a52 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IV Administration Set, Non-Toxic |
Version Model Number | 7045 |
Company DUNS | 008124539 |
Company Name | DYNAREX CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |