AccessGUDID - DEVICE: ZPower Rechargeable System for Hearing Aids (00811204030430)

GUDID

Device Identifier (DI) Information

Brand Name: ZPower Rechargeable System for Hearing Aids
Version or Model: Z701-312
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 9-06-00109-05-NA
Company Name: ZPOWER, LLC

Primary DI Number: 00811204030430
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 061455809 *Terms of Use

Device Description: ZPower Rechargeable System for Hearing Aids Kit. Includes 1 Charger (00811204030577), 2 Battery Door Modules (00811204030560), 2 Silver-Zinc Batteries, and 1 AC Adapter

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:	No
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?
17115	Noninvasive device battery charger	An electrically-powered device designed to supply an electrical charge, via a direct/wired or wireless connection, to the battery of a noninvasive device to recharge it for operation; it is not intended to receive data from and transmit data to other devices (i.e., not a transceiver). It is typically in the form of an electronic circuitry housing with a cable.	Active	false
58185	Cochlear implant/auditory brainstem implant battery	An external component of a cochlear implant (CI) or auditory brainstem implant system designed to supply direct current (DC) to operate the electrically-powered and dependent components of the system. It is typically worn behind-the-ear (BTE), or is neck- or waist-worn, and may include an on/off switch. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OSM	Hearing Aid, Air Conduction With Wireless Technology
ESD	Hearing Aid, Air Conduction

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
Storage Environment Temperature: between 14 and 122 Degrees Fahrenheit
Handling Environment Temperature: between 50 and 104 Degrees Fahrenheit
Handling Environment Humidity: between 20 and 75 Percent (%) Relative Humidity
Handling Environment Atmospheric Pressure: more than 11 KiloPascal

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: Cell Size 312

Device Record Status

Public Device Record Key: 3c0b41a2-0bc0-4431-b412-78e5ef4b768c
Public Version Date: April 08, 2022
Public Version Number: 3
DI Record Publish Date: May 01, 2019