Primary Device ID | 18800003006042 |
NIH Device Record Key | d2e5ecab-60db-4f52-b4d2-9d4a82e66d9d |
Commercial Distribution Discontinuation | 2022-11-03 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | RAYDENT C&B |
Version Model Number | RCB05P |
Company DUNS | 690324087 |
Company Name | Ray Co., Ltd |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
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 |