AccessGUDID - DEVICE: ClearLine MD (00863193000321)

GUDID

Device Identifier (DI) Information

Brand Name: ClearLine MD
Version or Model: Part#:2240
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: ANESTHESIA SAFETY PRODUCTS, LLC

Primary DI Number: 00863193000321
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 40
Labeler D-U-N-S® Number*: 364188032 *Terms of Use

Device Description: ClearLine MD Disposable Cartridge with Collection Bag (the new product name of AirPurge System - Disposable unit), is a sterile, single use cartridge, shall be used with ClearLine IV.

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?
58977	Basic intravenous administration set, noninvasive	A collection of noninvasive devices intended to conduct fluids from an intravenous (IV) administration bag/bottle to a peripheral venous cannula (not included) during gravitational or pump administration to a patient's venous system; some types may in addition be intended for enteral feeding applications. It typically includes tubing, connectors, chambers, and clamps; the bag/bottle may be included. It neither includes devices intended for invasive use nor a heat exchanger. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OKL	Intravascular Administration Set, Automated Air Removal System

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
DEN080009	000

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 458df4e6-b50a-4964-aee3-b8b56723df9e
Public Version Date: April 07, 2021
Public Version Number: 5
DI Record Publish Date: September 23, 2016