FDA UDI In Commercial Distribution 🇺🇸 United States

Vistafix

DI: 09321502021722 · Model: 93101 · Cochlear Bone Anchored Solutions AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vistafix
Primary DI
09321502021722
Version / Model
93101
Catalog Number
93101
Company Name
Cochlear Bone Anchored Solutions AB
Labeler DUNS
559784736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-22
Public Version
4
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
66197e29-4103-4522-9aa9-5d4a3f99fb6d

Device Description

Cochlear™ Vistafix® VXI300 Implant 4mm

Device Characteristics

Single Use
Yes
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 Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
FZE PROSTHESIS, NOSE, INTERNAL

GMDN Terms

Code Name
46638 Craniofacial bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 09321502021722

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K945154 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Implant 4 mm
Length 4 Millimeter