FDA UDI Not in Commercial Distribution 🇺🇸 United States

Kick®

DI: 04056481006570 · Model: 18078 · Brainlab AG
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kick®
Primary DI
04056481006570
Version / Model
18078
Catalog Number
18078
Company Name
Brainlab AG
Labeler DUNS
314482980
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-15
Public Version
6
Public Version Date
2023-01-31
Public Version Status
Update
Public Device Record Key
2eba7535-35f9-4f0d-a95a-94b0645303f7
Distribution End Date
2022-12-19

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
Labeling does not contain MRI Safety Information
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
No

Product Codes

Code Name
HAW Neurological Stereotaxic Instrument
OLO Orthopedic Stereotaxic Instrument

GMDN Terms

Code Name
38723 Robotic surgical navigation system

Identifiers

Type ID
Primary 04056481006570

Customer Contacts

Phone
+49899915680

Premarket Submissions

Submission Number Supplement Number
K092467 000
K183605 000