| Primary Device ID | 00733657201529 |
| NIH Device Record Key | 7d1fdf53-fa8f-4a5e-b3f3-74790d25e06c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SINGLE LOOP PREPPER |
| Version Model Number | 937058 |
| Company DUNS | 056007248 |
| Company Name | ALIMED, INC. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | true |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00733657201529 [Primary] |
| BWN | TABLE AND ATTACHMENTS, OPERATING-ROOM |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-12-09 |
| Device Publish Date | 2022-12-01 |