| Primary Device ID | 00840194471930 |
| NIH Device Record Key | c64725af-13a0-4f2b-b8f5-c4f96d2597de |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DF2 |
| Version Model Number | 03-DF2B-0156 |
| Catalog Number | 03-DF2B-0156 |
| Company DUNS | 796416191 |
| Company Name | ORTHOPEDIATRICS CORP. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840194471930 [Primary] |
| IQI | ORTHOSIS, LIMB BRACE |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-07-18 |
| Device Publish Date | 2024-07-10 |
| 00840194471930 | Cool Foam Pad, Right, XXL |
| 00840194471916 | Cool Foam Pad, Left, XXL |
| 00840194471909 | Cool Foam Pad, Right, XL |
| 00840194471893 | Cool Foam Pad, Left, XL |
| 00840194471879 | Cool Foam Pad, Right, L |
| 00840194471862 | Cool Foam Pad, Left, L |
| 00840194471855 | Cool Foam Pad, Right, M |
| 00840194471831 | Cool Foam Pad, Left, M |
| 00840194471824 | Cool Foam Pad, Right, S |
| 00840194471817 | Cool Foam Pad, Left, S |
| 00840194471794 | Cool Foam Pad, Right, XS |
| 00840194471787 | Cool Foam Pad, Left, XS |