Cirq Robotic Alignment Module 56100

GUDID 04056481141646

Brainlab AG

Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted Surgical instrument assist arm system, power-adjusted
Primary Device ID04056481141646
NIH Device Record Key73ec2839-1bc0-44a0-8e3f-2f3aaef83c4f
Commercial Distribution StatusIn Commercial Distribution
Brand NameCirq Robotic Alignment Module
Version Model Number56100
Catalog Number56100
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
GS104056481141646 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HAWNeurological Stereotaxic Instrument
OLOOrthopedic Stereotaxic Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-01-12
Device Publish Date2021-01-04

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