Primary Device ID | 08809708759980 |
NIH Device Record Key | 5b445193-3b8c-4b5b-ae28-e0d8ce0af430 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AnyRidge Int. Dummy (Marketing) |
Version Model Number | FANIHX4013 |
Catalog Number | M-DMFANIHX4013 |
Company DUNS | 687388178 |
Company Name | Megagen Implant Co. Ltd |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
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 |