Primary Device ID | 00848838022371 |
NIH Device Record Key | 2c2c7e6b-b300-43f6-af2f-291928eb3f4f |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | R21090 |
Company DUNS | 065769564 |
Company Name | REMEL, INC. |
Device Count | 25 |
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 | false |
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 |