Primary Device ID | D814SBL121 |
NIH Device Record Key | 9389155e-8a13-42b8-bef9-abead84ec25d |
Commercial Distribution Discontinuation | 2017-05-16 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | ProTech SuperBond |
Version Model Number | SBL12 |
Catalog Number | SBL12 |
Company DUNS | 117374900 |
Company Name | PROTECH PROFESSIONAL PRODUCTS 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 | 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 |