Primary Device ID | 20050428379367 |
NIH Device Record Key | 859598e5-e374-4754-8299-5c1c02dc64b5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CVS |
Version Model Number | DNE1317C1 |
Company DUNS | 062312574 |
Company Name | WOONSOCKET PRESCRIPTION CENTER, INCORPORATED |
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 | false |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00050428293416 [Primary] |
GS1 | 20050428379367 [Package] Contains: 00050428293416 Package: Case [6 Units] In Commercial Distribution |
GS1 | 30050428293417 [Package] Package: Shipper [24 Units] In Commercial Distribution |
LFD | Saliva, Artificial |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-08-16 |
Device Publish Date | 2022-08-08 |
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