Primary Device ID | 06430035420575 |
NIH Device Record Key | e2d73d6e-d833-479a-a370-0ebb4b1b9595 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Planmeca Compact |
Version Model Number | i5 |
Catalog Number | 30013450, 30015629, 30015630, 30015632, 30015633 |
Company DUNS | 368788568 |
Company Name | Planmeca Oy |
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 | false |
Serial Number | true |
Manufacturing Date | true |
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 |