Primary Device ID | 00311917016085 |
NIH Device Record Key | 225517e8-e33c-45e3-a14c-7354aa7f2fc7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WALGREEN |
Version Model Number | 875715 |
Company DUNS | 008965063 |
Company Name | WALGREEN CO. |
Device Count | 1 |
DM Exempt | true |
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 | 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 |
Phone | 800-925-4733 |
consumerrelations.pq@walgreens.corn | |
Phone | 800-925-4733 |
consumerrelations.pq@walgreens.corn | |
Phone | 800-925-4733 |
consumerrelations.pq@walgreens.corn | |
Phone | 800-925-4733 |
consumerrelations.pq@walgreens.corn | |
Phone | 800-925-4733 |
consumerrelations.pq@walgreens.corn | |
Phone | 800-925-4733 |
consumerrelations.pq@walgreens.corn | |
Phone | 800-925-4733 |
consumerrelations.pq@walgreens.corn |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00311917016085 [Primary] |
GS1 | 10311917016082 [Package] Package: CARTON [4 Units] In Commercial Distribution |
PUH | Analyzer, Body Composition, Exempt |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-08-09 |
Device Publish Date | 2021-07-30 |
00049022125926 | Compression Sleeve - Knee S/M |
00311917016085 | WALG DIGITAL GLASS SCALE 1S |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() WALGREEN 72216988 0817936 Dead/Expired |
WALGREEN CO. 1965-04-20 |
![]() WALGREEN 72216903 0817274 Dead/Expired |
WALGREEN CO. 1965-04-19 |