| Primary Device ID | 00840828194235 |
| NIH Device Record Key | 86706b16-b63e-4453-957d-12c754eae1cc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | REGO 1.1,PID,WT,PN,TL,FD,10' |
| Version Model Number | PD11-100400000A |
| Catalog Number | 27854 |
| Company DUNS | 796452311 |
| Company Name | CURBELL MEDICAL PRODUCTS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| 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 | true |
| Serial Number | false |
| 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 | false |
| Phone | 18002357500 |
| mwinter@curbell.com | |
| Phone | 18002357500 |
| mwinter@curbell.com | |
| Phone | 18002357500 |
| mwinter@curbell.com | |
| Phone | 18002357500 |
| mwinter@curbell.com | |
| Phone | 18002357500 |
| mwinter@curbell.com | |
| Phone | 18002357500 |
| mwinter@curbell.com | |
| Phone | 18002357500 |
| mwinter@curbell.com | |
| Phone | 18002357500 |
| mwinter@curbell.com | |
| Phone | 18002357500 |
| mwinter@curbell.com | |
| Phone | 18002357500 |
| mwinter@curbell.com | |
| Phone | 18002357500 |
| mwinter@curbell.com | |
| Phone | 18002357500 |
| mwinter@curbell.com | |
| Phone | 18002357500 |
| mwinter@curbell.com | |
| Phone | 18002357500 |
| mwinter@curbell.com | |
| Phone | 18002357500 |
| mwinter@curbell.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840828194235 [Primary] |
| ILQ | System, Communication, Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-03-07 |
| Device Publish Date | 2025-02-27 |