Primary Device ID | 00846468056087 |
NIH Device Record Key | ffb1e585-de3d-4a5d-8261-99737a1df10b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MaxFuse,VBR, 12 (D) x 14 (W) x 23 (H) |
Version Model Number | 62-1517-34 |
Catalog Number | 62-1517-34 |
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 |