| Primary Device ID | 00840314800091 |
| NIH Device Record Key | fd1aa9bc-4b8e-465d-9add-6598c4f1a0ec |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PARALLEL BAR,FLDNG,HT ADJ,SPEC CONST 2PC |
| Version Model Number | 1319-99 |
| Company DUNS | 001892660 |
| Company Name | Hausmann Enterprises, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Safe |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840314800091 [Primary] |
| IOE | Bars, Parallel, Exercise |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-08-24 |
| Device Publish Date | 2022-08-16 |
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