AccessGUDID - DEVICE: ViaMed (00811382011467)

GUDID

Device Identifier (DI) Information

Brand Name: ViaMed
Version or Model: 13410-MIX
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: RECE INTERNATIONAL CORPORATION

Primary DI Number: 00811382011467
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 100
Labeler D-U-N-S® Number*: 787828537 *Terms of Use

Device Description: Chest piece with two functions. The binaural head frame is made seamless brass tubes. Thick walled 22" PVC tubing, durable and noise proof. Comfortable smooth plastic ear plugs. Mixed Colors.

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):	Yes
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
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?
13755	Mechanical external stethoscope	A non-powered, external listening device designed to be placed on the patient’s skin to listen sounds from the arms, heart, lungs, and/or gastrointestinal tract. It typically comprises a membrane at the listening head connected by a split "Y" tube to the headgear with ear olives that are placed into the user’s ears. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LDE	Stethoscope, Manual

FDA Premarket Submission

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

Device Exempt from Premarket Submission: Yes 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: 14a2ead5-5906-4c67-b5ee-b81e66d69d1b
Public Version Date: November 25, 2024
Public Version Number: 2
DI Record Publish Date: November 27, 2020