AccessGUDID - DEVICE: FOGARTY (00690103043587)

GUDID

Device Identifier (DI) Information

Brand Name: FOGARTY
Version or Model: 2202310F
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 2202310F
Company Name: Edwards Lifesciences LLC

Primary DI Number: 00690103043587
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 134139174 *Terms of Use

Device Description: FOGARTY IRRIGATION CATHETER 10F, 23CM

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):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
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?
62649	Biliary/vascular irrigation catheter	A sterile, flexible, single-lumen tube intended to access the biliary system during open surgery to introduce fluids (e.g., saline) to irrigate the lumen following a procedure to remove debris (e.g., biliary stone removal); it might additionally be intended to access the peripheral vascular system to introduce fluids (e.g., heparinized solution) to remove debris (e.g., thrombectomy). The device is not intended for percutaneous or endoscopic access, and is not intended for drainage/suction or wound irrigation. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GBX	CATHETER, IRRIGATION

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: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: STORE IN A COOL, DRY PLACE.

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: USABLE LENGTH: 23CM, FRENCH SIZE: 10F (3.3MM)

Device Record Status

Public Device Record Key: 41d1dee2-d7f7-469d-b014-6fb66997e737
Public Version Date: February 21, 2019
Public Version Number: 3
DI Record Publish Date: September 03, 2016

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

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: Yes
Manufacturing Date: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(800)822-9637
Email: tech_support@edwards.com

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