FDA UDI In Commercial Distribution 🇺🇸 United States

Widex

DI: 05706069951950 · Model: M-XP 220 · Widex A/S
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Widex
Primary DI
05706069951950
Version / Model
M-XP 220
Catalog Number
21004691
Company Name
Widex A/S
Labeler DUNS
309843613
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-27
Public Version
1
Public Version Date
2021-04-05
Public Version Status
New
Public Device Record Key
382a313e-f8bc-44d4-8850-1dd10b0297b5

Device Description

WIDEX MAGNIFY M-XP 220 (Dark brown)

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OSM Hearing aid, air conduction with wireless technology

GMDN Terms

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

Identifiers

Type ID
Primary 05706069951950

Customer Contacts

Phone
+4544355600