Primary Device ID | B707128320050010 |
NIH Device Record Key | f39904f0-df87-4532-95a5-b4a0e1cb3015 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KIT DUALX LLIF 7-9MM x 0 DEG x 40MM |
Version Model Number | 12832005001 |
Company DUNS | 081021000 |
Company Name | Amplify Surgical, Inc. |
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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |