| Primary Device ID | 00733657283631 |
| NIH Device Record Key | f3be3424-e112-4aff-a898-e09d7ee4279d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | STRAP UNIVERSAL 4IN x 72IN 25/PK |
| Version Model Number | 753925 |
| Catalog Number | 2970009998 |
| Company DUNS | 056007248 |
| Company Name | ALIMED, INC. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| 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 | false |
| OTC Over-The-Counter | true |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com | |
| Phone | +1(781)329-2900 |
| customerservice@alimed.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00733657283631 [Primary] |
| GS1 | 00733657300208 [Unit of Use] |
| CCX | SUPPORT, PATIENT POSITION |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2024-02-19 |
| Device Publish Date | 2022-12-15 |