| 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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