FDA UDI In Commercial Distribution 🇺🇸 United States

Retone

DI: 16974308960094 · Model: K239RC · Xiamen Retone Hearing Technology Co., Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Retone
Primary DI
16974308960094
Version / Model
K239RC
Company Name
Xiamen Retone Hearing Technology Co., Ltd
Labeler DUNS
544329913
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-24
Public Version
2
Public Version Date
2025-02-13
Public Version Status
Update
Public Device Record Key
6b810176-e259-4e19-93e0-484cd1adff8d

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QUF Hearing Aid, Air-Conduction, Over The Counter

GMDN Terms

Code Name
34672 Air-conduction hearing aid, in-the-ear

Identifiers

Type ID
Primary 16974308960094