Primary Device ID | 00841494105457 |
NIH Device Record Key | 7085fc6c-821b-4498-a694-30630c2c904e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SUB MUCOSAL UPP Electrode |
Version Model Number | TEE229A |
Catalog Number | TEE229A |
Company DUNS | 079095245 |
Company Name | Ellman International |
Device Count | 2 |
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 | true |
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 | true |
OTC Over-The-Counter | false |