FDA UDI In Commercial Distribution 🇺🇸 United States

Oticon

DI: 05707131106964 · Model: 102-76-290-00 · Oticon A/S
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Oticon
Primary DI
05707131106964
Version / Model
102-76-290-00
Company Name
Oticon A/S
Labeler DUNS
305839946
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-19
Public Version
3
Public Version Date
2020-10-06
Public Version Status
Update
Public Device Record Key
07d32021-7760-4ab9-831e-9971dcc33ed6

Device Description

GO PRO, DEMO BTE D P RBE

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ESD Hearing aid, air conduction

GMDN Terms

Code Name
34671 Air-conduction hearing aid, behind-the-ear

Identifiers

Type ID
Primary 05707131106964

Customer Contacts

Phone
+4539177100