Primary Device ID | 20304040101852 |
NIH Device Record Key | 62370fe9-0249-40e2-8354-a2ea40154370 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Nytrile X300 Electra Blue PF Nitrile |
Version Model Number | 1127015 |
Catalog Number | 1127015 |
Company DUNS | 012430880 |
Company Name | HENRY SCHEIN, INC. |
Device Count | 300 |
DM Exempt | true |
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 | 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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Special Storage Condition, Specify | Between 0 and 0 *FALSE |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00304040101858 [Unit of Use] |
GS1 | 10304040101855 [Primary] |
GS1 | 20304040101852 [Package] Contains: 10304040101855 Package: [10 Units] In Commercial Distribution |
LZA | Polymer patient examination glove |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-01-16 |
Device Publish Date | 2020-01-08 |
20304040101838 | Nytrile X300 Electra Blue PF Nitrile LARGE |
20304040101876 | Nytrile X300 Electra Blue PF Nitrile MEDIUM |
20304040101869 | Nytrile X300 Electra Blue PF Nitrile X-SMALL |
20304040101852 | Nytrile X300 Electra Blue PF Nitrile SMALL |
20304040101845 | Nytrile X300 Electra Blue PF Nitrile X-LARGE |
H65811270192 | Nytrile X300 Electra Blue PF Nitrile X-LARGE |
H65811270172 | Nytrile X300 Electra Blue PF Nitrile MEDIUM |
H65811270152 | Nytrile X300 Electra Blue PF Nitrile SMALL |
H65811270142 | Nytrile X300 Electra Blue PF Nitrile X-SMALL |
H65811270182 | Nytrile X300 Electra Blue PF Nitrile X-SMALL |