| Primary Device ID | 20815149021519 |
| NIH Device Record Key | fbfa8942-f924-456e-9f51-7899ed3afc6f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CORFLO SAFETY PEG Kit with snare |
| Version Model Number | 50-5320-S7 |
| Catalog Number | 50-5320-S7 |
| 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 |
| Device Size Text, specify | 0 |
| Special Storage Condition, Specify | Between 0 and 0 *No |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10815149021512 [Primary] |
| GS1 | 20815149021519 [Package] Contains: 10815149021512 Package: [2 Units] In Commercial Distribution |
| KNT | TUBES, GASTROINTESTINAL (AND ACCESSORIES) |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[20815149021519]
Ethylene Oxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-04-20 |
| Device Publish Date | 2016-07-28 |
| 20815149021663 | PEG Kit with ENFit connectors Pull Technique with snare |
| 20815149021649 | PEG Kit with ENFit Connectors Pull Technique with Snare |
| 20815149021519 | PEG Safety Kit with ENFit Connectors Pull Technique with snare |