Primary Device ID | 00852371006118 |
NIH Device Record Key | a139b0a0-fd28-4495-a5d2-7629268150d7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Silhouette |
Version Model Number | SIL-090 |
Catalog Number | SIL-090 |
Company DUNS | 827042487 |
Company Name | BIOSTRUCTURES, LLC |
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 | 00852371006118 [Primary] |
MQV | Filler, Bone Void, Calcium Compound |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00852371006118]
Radiation Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-12-21 |
00852371006118 | Mineralized Collagen Strip |
00852371006101 | Mineralized Collagen Strip |