Primary Device ID | D9498180022 |
NIH Device Record Key | 690adc4f-528c-4a74-9444-1d9c48164e8a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Biofit HD Posterior Kit |
Version Model Number | Assorted 10ct |
Company DUNS | 059020838 |
Company Name | Bioclear Matrix Systems |
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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |