AccessGUDID - DEVICE: V. Mueller (10885403166914)

GUDID

Device Identifier (DI) Information

Brand Name: V. Mueller
Version or Model: U-0611
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: U-0611
Company Name: CAREFUSION 2200, INC

Primary DI Number: 10885403166914
Issuing Agency: GS1
Commercial Distribution End Date: October 01, 2016
Device Count: 1
Labeler D-U-N-S® Number*: 832696038 *Terms of Use

Device Description: CHROMA-LINE TAKA SUCTION TUBE XXL, 11FR, STR, LIGHT GREEN WORKING LENGTH 7" (180MM)

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:	No
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?
45254	Suction cannula, reusable	A rigid or semi-rigid, hand-held, metal or durable plastic tube designed as a conduit for the evacuation (suctioning) of blood, fluids, and other tissue debris directly from the surgical site during a surgical procedure (e.g., open-, plastic-, tissue/bone morcellation surgery). Also known as a suction tube, it is typically a general-purpose device to which the suction system tubing is connected proximally; some types may be attached to a dedicated handpiece that typically have a valve. Dedicated cannula specifically intended for a particular procedure (e.g., bronchial, dental, eye, uterine, oral, and liposuction) are also available. This is a reusable device.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
JOL	CATHETER AND TIP, SUCTION

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: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 861bc32a-60a3-48ec-8fcf-2ccb78461b3e
Public Version Date: March 29, 2018
Public Version Number: 2
DI Record Publish Date: September 24, 2016