| Primary Device ID | 20815149024091 |
| NIH Device Record Key | 7f64649a-b9fe-43c4-8eef-8b170bd2ce79 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CORFLO SAFETY PEG Kit |
| Version Model Number | 30-5320 |
| Catalog Number | 30-5320 |
| Company DUNS | 147530323 |
| Company Name | CORPAK MEDSYSTEMS, INC. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| 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 | +1(847)403-3400 |
| questions@corpak.com |
| Catheter Gauge | 20 French |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10815149024094 [Primary] |
| GS1 | 20815149024091 [Package] Contains: 10815149024094 Package: [2 Units] In Commercial Distribution |
| KNT | TUBES, GASTROINTESTINAL (AND ACCESSORIES) |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[20815149024091]
Ethylene Oxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-04-20 |
| Device Publish Date | 2016-08-04 |
| 20815149025432 | PEG Kit Pull Technique with snare |
| 20815149025425 | PEG Kit Pull Technique with Snare |
| 20815149025388 | PEG Safety Kit Pull Technique with snare |
| 20815149024206 | PEG Kit Pull Technique |
| 20815149024190 | PEG Kit Pull Technique |
| 20815149024091 | PEG Safety Kit Pull Technique |
| 20815149021656 | PEG Kit with ENFit Connectors Pull Technique |
| 20815149021632 | PEG Kit with ENFit Connectors Pull Technique |
| 20815149021502 | PEG Safety Kit with ENFit Connectors Pull Technique |