Primary Device ID | 20815149021496 |
NIH Device Record Key | ede67443-06b3-4bda-b2c0-d79c6cb3016b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CORFLO PEG Kit with snare |
Version Model Number | 50-5020-S7 |
Catalog Number | 50-5020-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 | 10815149021499 [Primary] |
GS1 | 20815149021496 [Package] Contains: 10815149021499 Package: [2 Units] In Commercial Distribution |
KNT | TUBES, GASTROINTESTINAL (AND ACCESSORIES) |
Steralize Prior To Use | true |
Device Is Sterile | true |
[20815149021496]
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 |
20815149025333 | PEG Kit Push Technique; with snare |
20815149024473 | PEG Kit with ENFit Connectors Pull Technique with snare |
20815149021571 | PEG Kit with ENFit Connectors Pull Technique with snare |
20815149021540 | PEG Kit with ENFit Connectors Pull Technique with snare |
20815149021496 | PEG Kit with ENFit connectors Pull Technique with snare |
20815149021489 | PEG Kit with ENFit connectors Pull Technique with snare |
20815149021434 | PEG Kit with ENFit connectors Push Technique; with snare |