Primary Device ID | E203USPU665 |
NIH Device Record Key | 4e98aa2e-88d2-4250-a08d-e832e32d6d48 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PGA RESORBA |
Version Model Number | PGA RESORBA |
Company DUNS | 341053195 |
Company Name | Resorba Medical GmbH |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |