PhenomTM 27 Catheter

GUDID 00847536041875

CATHETER FG15150-0630-1S V04

Micro Therapeutics, Inc.

Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use Vascular guide-catheter, single-use
Primary Device ID00847536041875
NIH Device Record Key314cc9b3-87c3-4448-b252-1f65efc13591
Commercial Distribution StatusIn Commercial Distribution
Brand NamePhenomTM 27 Catheter
Version Model NumberFG15150-0630-1S
Company DUNS826110710
Company NameMicro Therapeutics, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight Keep Dry

Device Identifiers

Device Issuing AgencyDevice ID
GS100847536041875 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KRACatheter, continuous flush

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-04-30
Device Publish Date2019-04-22

On-Brand Devices [PhenomTM 27 Catheter]

00847536041882CATHETER FG15160-0615-1S V04
00847536041875CATHETER FG15150-0630-1S V04
00847536041868CATHETER FG15150-0615-1S V04
00847536041851CATHETER FG15135-0615-1S V04
00763000399726CATHETER FG15160-0615-1S V06 US
00763000399719CATHETER FG15150-0630-1S V06 US
00763000399702CATHETER FG15150-0615-1S V06 US

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