Primary Device ID | 00850842006308 |
NIH Device Record Key | b8699f4c-806a-4157-9d84-ca8beccf30ec |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MOCACARE |
Version Model Number | Surgical Mask |
Company DUNS | 079824513 |
Company Name | MOCACARE CORP. |
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 | 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 | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850842006308 [Primary] |
FXX | Mask, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-05-08 |
Device Publish Date | 2023-04-30 |
00850842006308 | Surgical Mask |
00850842006292 | Procedure Mask |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MOCACARE 87940187 5648775 Live/Registered |
MOCACARE Corp 2018-05-29 |