AccessGUDID - DEVICE: Medline (10080196030897)

GUDID

Device Identifier (DI) Information

Brand Name: Medline
Version or Model: DYND12301
Commercial Distribution Status: In Commercial Distribution
Catalog Number: DYND12301
Company Name: MEDLINE INDUSTRIES, INC.

Primary DI Number: 10080196030897
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 025460908 *Terms of Use

Device Description: CATHETER,EXTERNAL,MALE,EXO,LTX,LG,35MM

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	Yes
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
32089	Cystographic/urethrographic catheter, male	A sterile, flexible or semi-rigid tube with one or more openings in the distal tip, designed to infuse a contrast medium into the male urethra, and possibly urinary bladder, for diagnostic radiographic imaging of the urethra and/or bladder. The imaging is typically used to delineate abnormalities of structure or function of the bladder and urethra, including the detection of vesicoureteral reflux and stress incontinence. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
NNX	DEVICE, INCONTINENCE, UROSHEATH TYPE, NON-STERILE

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: Store in cool, dry area. Protect from freezing, avoid excessive heat.

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 5b990c8c-b397-4491-b843-e5963da592e8
Public Version Date: January 07, 2021
Public Version Number: 1
DI Record Publish Date: December 30, 2020

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
40080196030898	25	10080196030897		In Commercial Distribution	CARTON

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: No
Expiration Date: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(800)633-5463
Email: service@medline.com

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