Primary Device ID | 00841034113270 |
NIH Device Record Key | fdb0fa66-58a9-4b44-924c-e9f158e0c193 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 3 LW SET 30" DU/SN DP - 10 |
Version Model Number | LDM305 |
Catalog Number | LDM305 |
Company DUNS | 066232067 |
Company Name | RPI |
Device Count | 10 |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |