| Primary Device ID | 00858836007065 |
| NIH Device Record Key | a2aede89-78f8-4382-9517-f5879b776074 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DiLumen C2 |
| Version Model Number | DiLumen C2.2 130 cm |
| Catalog Number | D-2004 |
| Company DUNS | 859290897 |
| Company Name | LUMENDI LLC |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 8444810822 |
| info@lumendi.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00858836007065 [Primary] |
| GS1 | 10858836007062 [Package] Package: Box [5 Units] In Commercial Distribution |
| FDF | Colonoscope And Accessories, Flexible/Rigid |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-01-03 |
| Device Publish Date | 2019-12-26 |
| 10865309000246 | DiLumen C2 consists of a soft flexible sheath that fits over standard endoscopes. The device emp |
| 10858836007031 | DiLumen C2 consists of a soft flexible sheath that fits over standard endoscopes. The device emp |
| 10858836007024 | DiLumen C2 consists of a soft flexible sheath that fits over standard endoscopes. The device emp |
| 00858836007089 | DiLumen C2 consists of a soft flexible sheath that fits over standard endoscopes. The device emp |
| 00858836007065 | DiLumen C2 consists of a soft flexible sheath that fits over standard endoscopes. The device emp |