Primary Device ID | D915MWH22 |
NIH Device Record Key | faff3003-63ce-407c-a8c7-2f69e8a7ffef |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sentinel |
Version Model Number | MWH2 |
Company DUNS | 079299604 |
Company Name | Plastcare USA |
Device Count | 50 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D915MWH20 [Unit of Use] |
HIBCC | D915MWH21 [Primary] |
HIBCC | D915MWH22 [Package] Contains: D915MWH21 Package: [20 Units] In Commercial Distribution |
FXX | Mask, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-05-06 |
Device Publish Date | 2019-12-12 |
D915MWH22 | Earloop Mask - White ASTM Level 2 |
D915MPI22 | Earloop Mask - Pink ASTM Level 2 |
D915MBL22 | Earloop Mask - Blue ASTM Level 2 |
D915MBK22 | Earloop Mask - Black ASTM Level 2 |