Primary Device ID | D080SSSOAXXL4XLXA40 |
NIH Device Record Key | f206f225-062d-49fe-8ab5-7d752f854bff |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SOLUUT PX |
Version Model Number | 6*1SET,L4,L,A4 |
Company DUNS | 693430001 |
Company Name | YAMAHACHI DENTAL MFG.,CO. |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |