Primary Device ID | 08809157488424 |
NIH Device Record Key | ee243860-7346-4df7-bce1-f035d8591223 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | C29000 |
Version Model Number | C29000 10P |
Company DUNS | 557822347 |
Company Name | B&B Company Co.,Ltd. |
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 | true |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |