SpeediCath Compact 28702

GUDID 05708932624688

SpeediCath Compact Male Kit. Compact with SpeediBag. Urinary catheter for intermittent catheterization. Ready to use coated catheter. Nelaton. Male. I

Coloplast A/S

Single-administration urethral drainage catheter Single-administration urethral drainage catheter Single-administration urethral drainage catheter Single-administration urethral drainage catheter Single-administration urethral drainage catheter Single-administration urethral drainage catheter Single-administration urethral drainage catheter Single-administration urethral drainage catheter Single-administration urethral drainage catheter Single-administration urethral drainage catheter Single-administration urethral drainage catheter Single-administration urethral drainage catheter Single-administration urethral drainage catheter
Primary Device ID05708932624688
NIH Device Record Key958bd7d8-715f-4964-ab9c-70087f39ed54
Commercial Distribution StatusIn Commercial Distribution
Brand NameSpeediCath Compact
Version Model Number28702
Catalog Number28702
Company DUNS305524696
Company NameColoplast A/S
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)533-0464
Emailhealthcarecs@coloplast.com
Phone+1(800)533-0464
Emailhealthcarecs@coloplast.com
Phone+1(800)533-0464
Emailhealthcarecs@coloplast.com
Phone+1(800)533-0464
Emailhealthcarecs@coloplast.com
Phone+1(800)533-0464
Emailhealthcarecs@coloplast.com
Phone+1(800)533-0464
Emailhealthcarecs@coloplast.com
Phone+1(800)533-0464
Emailhealthcarecs@coloplast.com
Phone+1(800)533-0464
Emailhealthcarecs@coloplast.com
Phone+1(800)533-0464
Emailhealthcarecs@coloplast.com
Phone+1(800)533-0464
Emailhealthcarecs@coloplast.com
Phone+1(800)533-0464
Emailhealthcarecs@coloplast.com
Phone+1(800)533-0464
Emailhealthcarecs@coloplast.com
Phone+1(800)533-0464
Emailhealthcarecs@coloplast.com

Device Dimensions

Catheter Gauge18 French
Catheter Gauge12 French
Outer Diameter4 Millimeter
Device Size Text, specify0
Outer Diameter6 Millimeter
Catheter Gauge18 French
Catheter Gauge12 French
Outer Diameter4 Millimeter
Device Size Text, specify0
Outer Diameter6 Millimeter
Catheter Gauge18 French
Catheter Gauge12 French
Outer Diameter4 Millimeter
Device Size Text, specify0
Outer Diameter6 Millimeter
Catheter Gauge18 French
Catheter Gauge12 French
Outer Diameter4 Millimeter
Device Size Text, specify0
Outer Diameter6 Millimeter
Catheter Gauge18 French
Catheter Gauge12 French
Outer Diameter4 Millimeter
Device Size Text, specify0
Outer Diameter6 Millimeter
Catheter Gauge18 French
Catheter Gauge12 French
Outer Diameter4 Millimeter
Device Size Text, specify0
Outer Diameter6 Millimeter
Catheter Gauge18 French
Catheter Gauge12 French
Outer Diameter4 Millimeter
Device Size Text, specify0
Outer Diameter6 Millimeter
Catheter Gauge18 French
Catheter Gauge12 French
Outer Diameter4 Millimeter
Device Size Text, specify0
Outer Diameter6 Millimeter
Catheter Gauge18 French
Catheter Gauge12 French
Outer Diameter4 Millimeter
Device Size Text, specify0
Outer Diameter6 Millimeter
Catheter Gauge18 French
Catheter Gauge12 French
Outer Diameter4 Millimeter
Device Size Text, specify0
Outer Diameter6 Millimeter
Catheter Gauge18 French
Catheter Gauge12 French
Outer Diameter4 Millimeter
Device Size Text, specify0
Outer Diameter6 Millimeter
Catheter Gauge18 French
Catheter Gauge12 French
Outer Diameter4 Millimeter
Device Size Text, specify0
Outer Diameter6 Millimeter
Catheter Gauge18 French
Catheter Gauge12 French
Outer Diameter4 Millimeter
Device Size Text, specify0
Outer Diameter6 Millimeter

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if sterile barrier is damaged
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if sterile barrier is damaged
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if sterile barrier is damaged
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if sterile barrier is damaged
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if sterile barrier is damaged
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if sterile barrier is damaged
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if sterile barrier is damaged
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if sterile barrier is damaged
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if sterile barrier is damaged
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if sterile barrier is damaged
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if sterile barrier is damaged
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if sterile barrier is damaged
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if sterile barrier is damaged
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight

Device Identifiers

Device Issuing AgencyDevice ID
GS105708932624671 [Primary]
GS105708932624688 [Package]
Contains: 05708932624671
Package: Shipper box [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GBMCATHETER, URETHRAL

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-24

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