Primary Device ID | 00841494103347 |
NIH Device Record Key | 8088973c-c0f9-4e15-bdf7-8b5d15b1080c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GLASS FIBRE POST |
Version Model Number | EGF202 |
Catalog Number | EGF202 |
Company DUNS | 079095245 |
Company Name | Ellman International |
Device Count | 6 |
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 | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |