AccessGUDID - DEVICE: Indeflator (08717648013607)

GUDID

Device Identifier (DI) Information

Brand Name: Indeflator
Version or Model: 1000185
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 1000185
Company Name: ABBOTT VASCULAR INC.

Primary DI Number: 08717648013607
Issuing Agency: GS1
Commercial Distribution End Date: January 16, 2023
Device Count: 1
Labeler D-U-N-S® Number*: 964569052 *Terms of Use

Device Description: PLUS 30 PRIORITY PACK Accessory Kit includes INDEFLATOR PLUS 30 Inflation Device 30 atm 10 cc / Rotating Hemostatic Valve .096 " / Guide Wire Introducer / Torque Device

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?
17541	Catheter/overtube balloon inflator, single-use	A device designed to inflate and regulate the pressure of the balloon of a catheter, endoscopic overtube, or other invasive device (e.g., tamp, endomicroscopy probe), typically by injecting and aspirating fluid or air within the balloon, and to deflate the balloon during a medical procedure. It typically consists of a dedicated manual syringe/plunger or electronic mechanism for inflation/deflation, an analogue or digital gauge/screen for monitoring pressure, a locking mechanism, and a connecting tube. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MAV	Syringe, balloon inflation

FDA Premarket Submission

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

Device Exempt from Premarket Submission: No 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 dry, dark, cool place.

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 01c23bb1-cf83-4e78-9c5e-ea1c9b9f6a08
Public Version Date: August 26, 2024
Public Version Number: 6
DI Record Publish Date: August 05, 2016