| Primary Device ID | 00850010866031 |
| NIH Device Record Key | 2608a2b6-b3b0-4206-adac-1e54502eb4b5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | iMed Technology Anchor Dry 7x7 |
| Version Model Number | iMed 7x7 |
| Company DUNS | 087974775 |
| Company Name | Imed Technology, Inc. |
| Device Count | 980 |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850010866031 [Unit of Use] |
| GS1 | 00850010866048 [Primary] |
| GS1 | 00850010866055 [Primary] |
| NAD | Dressing, Wound, Occlusive |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-01-06 |
| Device Publish Date | 2024-12-28 |
| 00850010866000 - iMed Technology Anchor Dry 5x5 | 2025-01-06 iMed Anchor Dry 5x5 Inner Box |
| 00850010866031 - iMed Technology Anchor Dry 7x7 | 2025-01-06iMed Anchor Dry 7x7 Master Carton |
| 00850010866031 - iMed Technology Anchor Dry 7x7 | 2025-01-06 iMed Anchor Dry 7x7 Master Carton |
| 00850010866062 - iMed Technology Anchor Dry 9x9 | 2025-01-06 iMed Anchor Dry 9x9 Master Carton |
| 00850010866093 - iMed Technology Anchor Dry 10x12 | 2025-01-06 iMed Anchor Dry 10x12 Master Carton |
| 00850010866123 - iMed Technology Anchor Dry 12x14 | 2025-01-06 iMed Anchor Dry 12x14 Master Carton |