Primary Device ID | 00813954020846 |
NIH Device Record Key | e14890a7-580d-4686-a87e-315d7207a293 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OssiMend BLOCK |
Version Model Number | MCCB0514 |
Company DUNS | 176262442 |
Company Name | COLLAGEN MATRIX, 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813954020846 [Primary] |
MQV | Filler, Bone Void, Calcium Compound |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-10-22 |
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00813954020860 | Bone Graft Matrix |
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00813954020846 | Bone Graft Matrix |
00813954020839 | Bone Graft Matrix |
00813954020822 | Bone Graft Matrix |
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00813954026886 | Bone Graft Matrix |