FDA UDI In Commercial Distribution 🇺🇸 United States

Localizer Bone Anchor

DI: EFIAE0122041 · Model: 1 · Fiagon GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Localizer Bone Anchor
Primary DI
EFIAE0122041
Version / Model
1
Company Name
Fiagon GmbH
Labeler DUNS
312623008
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-27
Public Version
4
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
a1246085-7f59-408b-a6f2-62d47e275fd6

Device Description

The product Localizer Bone Anchor is a product variant of a patient reference localisator for image guided surgical procedures for cranial indications.

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
No
PM Exempt
No
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HAW Neurological Stereotaxic Instrument

GMDN Terms

Code Name
45199 Multi-purpose stereotactic surgery system

Identifiers

Type ID
Direct Marking EFIAE01220410
Primary EFIAE0122041

Customer Contacts

Phone
+13364282241

Premarket Submissions

Submission Number Supplement Number
K163209 000

Storage Conditions

Type
Handling Environment Atmospheric Pressure
Temperature Range
70 – 106 KiloPascal
Type
Handling Environment Humidity
Temperature Range
30 – 75 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
15 – 35 Degrees Celsius