Primary Device ID | 00813954025056 |
NIH Device Record Key | 38961c36-1318-433e-8a1e-01c539a7d256 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Opus BA Putty |
Version Model Number | 71410205 |
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 | 00813954025056 [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 | 2022-09-15 |
Device Publish Date | 2022-09-07 |
00813954024493 | Osteoconductive Matrix |
00813954024486 | Osteoconductive Matrix |
00813954025070 | Osteoconductive Matrix |
00813954025063 | Osteoconductive Matrix |
00813954025056 | Osteoconductive Matrix |
00813954025049 | Osteoconductive Matrix |