AccessGUDID - DEVICE: Anesthesia/Breathing Circuits (00709078014512)

GUDID

Device Identifier (DI) Information

Brand Name: Anesthesia/Breathing Circuits
Version or Model: 9700
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: WESTMED, INC.

Primary DI Number: 00709078014512
Issuing Agency: GS1
Commercial Distribution End Date: May 31, 2024
Device Count: 1
Labeler D-U-N-S® Number*: 092673953 *Terms of Use

Device Description: 120" Adult 22mm/2mm Expandable Circuit, Parallel WYE, 2() B/V Filters, Mini HEMF W/ CO2 Port, Adult Vent Mask, 2L not made with latex breathing bag, Sterile Yankuer, W/Bulb Tip, 10' x 0.050 M/M GSL, 10' Suction Tubing

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":	Yes
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?
37704	Anaesthesia breathing circuit, single-use	An assembly of devices designed to conduct medical gases from an anaesthesia unit/workstation to a patient artificial airway/anaesthesia mask (not included) during general anaesthesia. It includes breathing tubes and a Y-piece connector, typically with a ventilator/ventilation bag and appropriate connectors, and may include a carbon dioxide (CO2) absorber, a one-way directional valve, or adjustable pressure limiting (APL) valve. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
CAH	Filter, Bacterial, Breathing-Circuit
OFP	Anesthesia Breathing Circuit Kit (Adult & Pediatric)

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K922492	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: 52c58ab8-9e8b-49cc-bcf6-5ba467d2555e
Public Version Date: May 31, 2024
Public Version Number: 4
DI Record Publish Date: May 31, 2022