Primary Device ID | 00812594013089 |
NIH Device Record Key | e7ca74c9-a91c-44bc-80e8-b40c62345ac9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NeoGlo Disposable |
Version Model Number | 10812594013086 |
Company DUNS | 198013435 |
Company Name | NEOTECH PRODUCTS, INC. |
Device Count | 10 |
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 | 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 |