| Primary Device ID | 10850014574205 |
| NIH Device Record Key | 9382eba5-a165-4e6f-9f36-3465b3e342ea |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Foley Loc |
| Version Model Number | 650 |
| Catalog Number | 650 |
| Company DUNS | 622637098 |
| Company Name | PEPPER MEDICAL INC. |
| Device Count | 50 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| 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 | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com | |
| Phone | +1(800)647-0172 |
| gschuster@peppermedical.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850014574208 [Primary] |
| GS1 | 10850014574205 [Unit of Use] |
| EYJ | HOLDER, URETERAL CATHETER |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-04-27 |
| Device Publish Date | 2020-04-17 |
| 10850014574205 | Multi Tube Holder |
| 00850014574208 | Multi Tube Holder |