| Primary Device ID | 00708820519558 |
| NIH Device Record Key | bb543955-bf53-4193-8a4b-51d160b24ddb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Meijer Hot & Cold Wrap Ultra-Forming |
| Version Model Number | 3457246 |
| Company DUNS | 006959555 |
| Company Name | MEIJER, INC. |
| 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 | true |
| 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 | 630-481-1000 |
| jeff@bigwall.us | |
| Phone | 630-481-1000 |
| jeff@bigwall.us |
| Area/Surface Area | 93 Square inch |
| Area/Surface Area | 93 Square inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00708820519558 [Primary] |
| IME | Pack, Hot Or Cold, Reuseable |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-08-01 |
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