AccessGUDID - DEVICE: Pole Mount for use with VTI TQI Doppler, Gen 0.5 (00817122020584)

GUDID

Device Identifier (DI) Information

Brand Name: Pole Mount for use with VTI TQI Doppler, Gen 0.5
Version or Model: 201455
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 201455
Company Name: VASCULAR TECHNOLOGY, INCORPORATED

Primary DI Number: 00817122020584
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 161989343 *Terms of Use

Device Description: Part Number 201455, Pole Mount for use with VTI TQI Doppler, Gen 0.5

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):	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?
61952	Frame/rail/pole device holder	A clamp-like device intended to be affixed to a bed frame, standard rail or standing pole [e.g., intravenous (IV) pole] to provide a means to fix/mount a medical device (e.g., suction/irrigation pump, display monitor), or other non-medical device, to the support. It typically has a gripping profile that is compatible with the device it is intended to fit. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
DPW	FLOWMETER, BLOOD, CARDIOVASCULAR

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K082870	000

Device Exempt from Premarket Submission: No 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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: dfbb4351-eaa9-4ee0-b01c-0b8f3d5dc477
Public Version Date: May 30, 2025
Public Version Number: 2
DI Record Publish Date: January 25, 2024