Primary Device ID | 00856879006304 |
NIH Device Record Key | 72cf23d9-7c31-4152-b91b-76c4e7e36626 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FIBERGRAFT Aeridyan Matrix |
Version Model Number | 59000030 |
Catalog Number | 59000030 |
Company DUNS | 963425488 |
Company Name | PROSIDYAN, 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 | true |
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 |
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00856879006304 | Aeridyan Matrix Bone Graft Substitute, Small, 3cc |
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00856879006281 | Aeridyan Matrix Bone Graft Substitute, Medium, 6.25cc |
00856879006250 | Aeridyan Matrix Bone Graft Substitute, Large, 12.5cc |
00856879006946 | Aeridyan Matrix Bone Graft Substitute, X-Large, 20cc |
00856879006922 | Aeridyan Matrix Bone Graft Substitute, Large, 12.5cc |
00856879006915 | Aeridyan Matrix Bone Graft Substitute, Medium, 6.25cc |
00856879006908 | Aeridyan Matrix Bone Graft Substitute, Small, 3cc |