| Primary Device ID | 00850051939541 |
| NIH Device Record Key | 1ba4cf1b-7823-4831-b0db-f9c5ecb683f8 |
| Commercial Distribution Discontinuation | 2030-05-18 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CopperUnder sock Extra Large |
| Version Model Number | AW7025-02 |
| Catalog Number | CS400 |
| Company DUNS | 609397224 |
| Company Name | SUN SCIENTIFIC, 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | true |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com | |
| Phone | 9144795108 |
| aalward@sun-scientific.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850051939541 [Primary] |
| LLK | Legging, Compression, Non-Inflatable |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-09-18 |
| Device Publish Date | 2024-09-10 |
| 00850051939565 - AeroWrap™ Full Leg | 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k |
| 00850051939572 - AeroWrap™ Full Leg | 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k |
| 00850051939589 - AeroWrap™ Full Leg | 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k |
| 00850051939596 - AeroWrap™ Full Leg | 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k |
| 00850051939602 - AeroWrap™ Full Leg | 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k |
| 00850051939619 - AeroWrap™ Full Leg | 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k |
| 00850051939626 - AeroWrap™ Full Leg | 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k |
| 00850051939640 - AeroWrap™ Full Leg | 2024-12-13 The AeroWrap ™ Full Leg System is comprised of inflatable gradient compression sleeves, a Brace sleeve from the ankle to the k |