FDA UDI In Commercial Distribution 🇺🇸 United States

LEKSELL FRAME REGISTRATION PLATES

DI: 03760244034069 · Model: 174016-01 · MEDTECH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LEKSELL FRAME REGISTRATION PLATES
Primary DI
03760244034069
Version / Model
174016-01
Catalog Number
ROSAS00500
Company Name
MEDTECH
Labeler DUNS
264502977
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-20
Public Version
3
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
162c4f41-a4d5-46d5-aa32-c77236a2a059

Device Description

Leksell Registration Plates instrument Rosa One 3.1 (brain application) Leksell frame regsitration plates : calibrated tool for manual regsitration of the device with the leksell frame. Mounted on the leksell stereotactic frame.

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HAW Neurological Stereotaxic Instrument

GMDN Terms

Code Name
45199 Multi-purpose stereotactic surgery system

Identifiers

Type ID
Primary 03760244034069

Premarket Submissions

Submission Number Supplement Number
K200511 000