Primary Device ID | 20815149021076 |
NIH Device Record Key | 050da6a4-8d2d-459f-80a9-78a5fdd8bd14 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CORFLO Gastrostomy Tube |
Version Model Number | 52-2022 |
Catalog Number | 52-2022 |
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 | 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 | +1(847)403-3400 |
questions@corpak.com |
Total Volume | 20 Milliliter |
Special Storage Condition, Specify | Between 0 and 0 *No |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10815149021079 [Primary] |
GS1 | 20815149021076 [Package] Contains: 10815149021079 Package: [2 Units] In Commercial Distribution |
KNT | TUBES, GASTROINTESTINAL (AND ACCESSORIES) |
Steralize Prior To Use | true |
Device Is Sterile | true |
[20815149021076]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-04-20 |
Device Publish Date | 2016-06-24 |
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