VarioGuide Disc Set Cranial Drill Kit

GUDID 04056481144012

Brainlab AG

Surgical instrument assist arm system, manually-adjusted
Primary Device ID04056481144012
NIH Device Record Key9e390b8b-cafd-41cc-9d86-7670e289714f
Commercial Distribution StatusIn Commercial Distribution
Brand NameVarioGuide Disc Set Cranial Drill Kit
Version Model Number55956-31
Company DUNS314482980
Company NameBrainlab AG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104056481144012 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HAWNeurological Stereotaxic Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


[04056481144012]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-09-26
Device Publish Date2023-09-18

Devices Manufactured by Brainlab AG

04056481144906 - Spine &Trauma Navigation2024-11-22
04056481146238 - PATIENT REFERENCE ARRAY SPINE & TRAUMA2024-11-22
04056481146603 - ADAPTER SHORT FOR PATIENT REFERENCE CLAMP2024-11-22
04056481146610 - ADAPTER X-PRESS FOR PATIENT REFERENCE ARRAY2024-11-22
04056481143916 - Spine Planning2024-11-13
04056481144654 - Viewer 5.42024-11-13
04056481143527 - DICOM Proxy2024-11-01
04056481144913 - CRANIAL 4PI STEREOTACTIC MASK (5 PCS.)2024-07-26

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.