Primary Device ID | 07333066011523 |
NIH Device Record Key | 52b89fe8-41f3-4380-b9a4-f50386fb9fe6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Stop Solution |
Version Model Number | 34-2271-51 |
Catalog Number | 34-2271-51 |
Company DUNS | 354019424 |
Company Name | Phadia AB |
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 | false |
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 | true |
OTC Over-The-Counter | false |