Primary Device ID | 80070942007296 |
NIH Device Record Key | d28d7ba5-e6c1-4e83-80ff-154ed81828fa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GUM |
Version Model Number | 90291 |
Catalog Number | R |
Company DUNS | 025066358 |
Company Name | SUNSTAR AMERICAS, INC. |
Device Count | 28 |
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 | false |
Serial Number | false |
Manufacturing Date | false |
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 | true |