Primary Device ID | 07640167750818 |
NIH Device Record Key | 69859592-5010-46b6-92a1-58452dfefbdb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FEMTO LDVᵀᴹ Intershields |
Version Model Number | d330 |
Catalog Number | 510.710.317 |
Company DUNS | 482163628 |
Company Name | SIE AG, Surgical Instrument Engineering |
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 | 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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |