RUSCH

Primary DI
34026704663461
Brand
RUSCH
Company
TELEFLEX INCORPORATED
Model
IPN039003
Catalog number
343103
Device description
Disposable
Published
2019-06-07
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Related Records

Contact Domains

Product Codes

CodeName
FBWFILIFORM AND FILIFORM FOLLOWER

Product Code Classifications

CodeDeviceSpecialtyClass
FBWFiliform And Filiform FollowerGastroenterology, Urology1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
24026704663464PackageGS110In Commercial Distribution
34026704663461PackageGS16In Commercial Distribution
04026704542901PreviousGS10
14026704663467PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedEAN-13
2402670466346424026704663464
3402670466346134026704663461
04026704542901040267045429014026704542901
1402670466346714026704663467

GMDN Terms

TermDefinition
Indwelling urethral drainage catheterA sterile, flexible tube with an inflatable balloon at its distal tip intended to be inserted through the urethra and retained in the urinary bladder, or prostatic bed, to function as an indwelling therapeutic device for urinary drainage; it might be designed to also allow for infusion of fluids (irrigation). It may have a bent tip (coude) to facilitate insertion, and some types may be provided with a guidewire to facilitate difficult insertion (e.g., in cases of enlarged prostate); it does not include an antimicrobial agent(s). Most types are commonly known as a Foley catheter; it is intended to be introduced by a healthcare professional. This is a single-use device.

Device Sizes

TypeValueUnit
Height0.01Inch
Length19Inch
Width2.9Inch

Storage And Handling

TypeLowHighCondition
Special Storage Condition, Specify00false
Special Storage Condition, Specify00None

Sterilization Methods

Method

Contacts

PhoneEmail
+1(919)544-8000CS@TELEFLEX.COM

Regulatory Flags

DUNS number
002348191
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

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