| Primary Device ID | 00817369021269 |
| NIH Device Record Key | 1077706f-013f-4395-a6f6-fbb50c1ebe84 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pulse Pro Upper and Lower Body Recovery Package |
| Version Model Number | Pulse Pro Recovery Package - Upper and Lower Body |
| Catalog Number | 40230 |
| Company DUNS | 111448069 |
| Company Name | NORMATEC INDUSTRIES LP |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817369021269 [Primary] |
| IRP | Massager, Powered Inflatable Tube |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-13 |
| 00817369021313 | Pulse Pro Recovery Package - Upper and Lower Body Power Tall |
| 00817369021306 | Pulse Pro Recovery Package - Upper and Lower Body Power Standard |
| 00817369021290 | Pulse Pro Recovery Package - Upper and Lower Body Power Short |
| 00817369021283 | Pulse Pro Recovery Package - Upper and Lower Body Short |
| 00817369021276 | Pulse Pro Recovery Package - Upper and Lower Body Tall |
| 00817369021269 | Pulse Pro Recovery Package - Upper and Lower Body Standard |