Primary Device ID | 00813954024974 |
NIH Device Record Key | e8ef9f5e-372a-464d-9b25-79e9391b8733 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BoneSync BioActive |
Version Model Number | ABS-3500-10 |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813954024974 [Primary] |
MQV | Filler, Bone Void, Calcium Compound |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-09-12 |
Device Publish Date | 2022-09-02 |
00813954025032 | Matrix Putty |
00813954025025 | Matrix Putty |
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00813954024998 | Matrix Strip |
00813954024981 | Matrix Strip |
00813954024974 | Matrix Strip |
00813954024967 | Matrix Strip |
00813954025438 | Matrix Putty |
00813954025582 | Matrix Strip |
00813954025575 | Matrix Strip |
00813954025568 | Matrix Strip |
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00813954025414 | Matrix Putty |