Primary Device ID | 10760236212062 |
NIH Device Record Key | d0080770-4056-45f7-b4df-b765b42ae6e6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Meijer Blister Guard Spray |
Version Model Number | 4705763 |
Company DUNS | 006959555 |
Company Name | MEIJER, INC. |
Device Count | 1 |
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 | 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 | 00760236212065 [Primary] |
GS1 | 10760236212062 [Package] Contains: 00760236212065 Package: Case [48 Units] In Commercial Distribution |
NEC | Bandage, Liquid, Skin Protectant |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-08 |
Device Publish Date | 2020-06-30 |
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