Primary Device ID | 00001182254533 |
NIH Device Record Key | 9e6ce0a9-0f00-44ed-a348-861210039c70 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Multi-Purpose Disinfecting Solution |
Version Model Number | 049 |
Company DUNS | 014578892 |
Company Name | RITE AID CORPORATION |
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 | 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 | 00001182254533 [Primary] |
LPN | Accessories, Soft Lens Products |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-12-18 |
Device Publish Date | 2019-12-10 |
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