FDA UDI In Commercial Distribution 🇺🇸 United States

Oticon

DI: 05714464006441 · Model: 219642 · Sbo Hearing A/S
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Oticon
Primary DI
05714464006441
Version / Model
219642
Company Name
Sbo Hearing A/S
Labeler DUNS
306018410
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-16
Public Version
2
Public Version Date
2022-08-04
Public Version Status
Update
Public Device Record Key
6a455a57-286a-4744-a4fa-828d02c87be1

Device Description

OTICON REMOTECARE 3.1.0 ANDROID

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KLW Masker, tinnitus
OSM Hearing aid, air conduction with wireless technology

GMDN Terms

Code Name
57885 Hearing aid/implant system remote control

Identifiers

Type ID
Primary 05714464006441

Customer Contacts

Phone
+4539177100