Primary Device ID | 10050428617653 |
NIH Device Record Key | 2e53328f-7255-484a-a1c5-2b7292b63cd1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CVS Liquid Bandage Spray |
Version Model Number | 276670 |
Company DUNS | 062312574 |
Company Name | WOONSOCKET PRESCRIPTION CENTER, INCORPORATED |
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 | 00050428617656 [Primary] |
GS1 | 10050428617653 [Package] Contains: 00050428617656 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 | 2020-01-23 |
Device Publish Date | 2020-01-15 |
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