Drill Guide Tube 3.2 X 150 Mm 41839-30A

GUDID 04056481003463

Brainlab AG

Robotic surgical navigation system
Primary Device ID04056481003463
NIH Device Record Keya0f5ddfb-e782-42db-a679-8de96c009f41
Commercial Distribution StatusIn Commercial Distribution
Brand NameDrill Guide Tube 3.2 X 150 Mm
Version Model Number41839-30A
Catalog Number41839-30A
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

Customer Support Contacts

Phone+49899915680
Emailcontact@brainlab.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104056481003463 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OLOOrthopedic Stereotaxic Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04056481003463]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-15

On-Brand Devices [Drill Guide Tube 3.2 X 150 Mm]

0405648113952041839-30B
0405648100346341839-30A

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.