AccessGUDID - DEVICE: Astraguard (B279F0502100)

GUDID

Device Identifier (DI) Information

Brand Name: Astraguard
Version or Model: Kushion Klip,Pneumoguard Adapter
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: F0502-100
Company Name: S D I DIAGNOSTICS INC

Primary DI Number: B279F0502100
Issuing Agency: HIBCC
Commercial Distribution End Date: March 26, 2019
Device Count: 100
Labeler D-U-N-S® Number*: 037690120 *Terms of Use

Device Description: Bacterial Viral Filter

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):	No
Over the Counter (OTC):	No
Kit:	Yes
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?
44545	Breathing mouthpiece, single-use	A device designed for partial insertion into a patient's mouth (in between the lips) to facilitate access to the respiratory system. It is typically a small rigid or semi-rigid plastic hollow device with a shape and structure that enables an appropriate gastight seal and prevents collapse. It is typically attached, either directly or through other tubes/adaptors, to diagnostic and/or therapeutic respiratory devices (e.g., ventilator, inhaler, incentive spirometer, aerosol equipment, breath analyser, breath collector); connectors and filters may be included with the device. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
BZG	Spirometer, Diagnostic

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K062913	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: e57bc59b-51c3-4d44-8be6-78f3ee7dc0f5
Public Version Date: July 06, 2023
Public Version Number: 6
DI Record Publish Date: September 13, 2016