Primary Device ID | 00846468055059 |
NIH Device Record Key | 56b0416d-b6a1-4f5f-b9e3-c3d0bfd66e1d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MaxFuse VBR, 10 (D) x 12 (W) x 25 (H) |
Version Model Number | 62-1012-39 |
Catalog Number | 62-1012-39 |
Company DUNS | 793384496 |
Company Name | Pioneer Surgical Technology, 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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |