Primary Device ID | 10884523003758 |
NIH Device Record Key | 3ee2ffb4-90ba-4aab-8347-6617b4158e22 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Multifire Endo SGIA |
Version Model Number | 030333 |
Catalog Number | 030333 |
Company DUNS | 058614483 |
Company Name | Covidien LP |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Height | 2.5 Millimeter |
Length | 30 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10884523003758 [Primary] |
GS1 | 20884523003755 [Package] Package: CASE [12 Units] In Commercial Distribution |
GDW | STAPLE, IMPLANTABLE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-05-07 |
Device Publish Date | 2015-05-25 |
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