WALGREEN
GUDID 00049022125926
Compression Sleeve - Knee S/M
WALGREEN CO.
Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable Tubular support bandage, non-latex, reusable| Primary Device ID | 00049022125926 |
| NIH Device Record Key | 7fc8e705-c359-43e7-81db-9e58b6467422 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | WALGREEN |
| Version Model Number | 107249 |
| Company DUNS | 008965063 |
| Company Name | WALGREEN CO. |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00049022125926 [Primary] |
| GS1 | 01049022125925 [Package] Package: Inner Pack [6 Units] In Commercial Distribution |
FDA Product Code
| IQI | Orthosis, Limb Brace |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-07-09 |
| Device Publish Date | 2020-07-01 |
On-Brand Devices [WALGREEN]
| 00049022125926 | Compression Sleeve - Knee S/M |
| 00311917016085 | WALG DIGITAL GLASS SCALE 1S |
Trademark Results [WALGREEN]
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 |
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