| Primary Device ID | 00817369020675 |
| NIH Device Record Key | 23e0f976-b7f0-42d9-bd29-5a481011991a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Carry Case |
| Version Model Number | Carry Case - Pulse |
| Catalog Number | 30301 |
| 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 | 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817369020675 [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 |
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| 00810050281751 - NormaTec | 2025-08-04 NT3 Control Unit (only) |
| 00810050288026 - Hyperice / NormaTec | 2025-08-04 HYPERICE X2 KNEE |
| 00810050288033 - Hyperice / NormaTec | 2025-08-04 HYPERICE X2 SHOULDER |
| 00810050281713 - NormaTec | 2024-08-05 Normatec Hose Attachment |
| 00810050281812 - NormaTec | 2024-08-05 Normatec right arm attachment |
| 00810050286053 - NormaTec | 2024-05-31 Normatec Elite standard leg system is a powered air pressure inflatable tube massager. It is intended to temporarily relieve min |
| 00810050281997 - NormaTec | 2024-05-21 Normatec 3 is a powered air pressure inflatable tube massager. It is intended to temporarily relieve minor muscle aches and / o |