3D X-RAY PATTERN ROSAS00499

GUDID 03760244031785

3D X-RAY PATTERN instrument Rosa one 3.1 (spine application) Calibrated device to register intraoperative 3D exams"

MEDTECH

Multi-purpose stereotactic surgery system
Primary Device ID03760244031785
NIH Device Record Keya478097b-4f27-47fe-90a6-6542b4453d9c
Commercial Distribution StatusIn Commercial Distribution
Brand Name3D X-RAY PATTERN
Version Model Number174021-01
Catalog NumberROSAS00499
Company DUNS264502977
Company NameMEDTECH
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
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
GS103760244031785 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OLOOrthopedic Stereotaxic Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


[03760244031785]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-12-26
Device Publish Date2019-12-18

On-Brand Devices [3D X-RAY PATTERN]

037602440304433D X-RAY PATTERN instrument Rosa one (spine application) Calibrated device to register intraoper
037602440317853D X-RAY PATTERN instrument Rosa one 3.1 (spine application) Calibrated device to register intra
037602440333833D X-RAY PATTERN instrument Rosa one 3.1 (spine application) Calibrated device to register intra

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