TMJ COIL N. 15

GUDID 08056304452634

ESAOTE SPA

MRI system coil, radio-frequency
Primary Device ID08056304452634
NIH Device Record Keyefce3247-fb2d-4fcd-b9dd-13a965d71b28
Commercial Distribution StatusIn Commercial Distribution
Brand NameTMJ COIL N. 15
Version Model Number229003500
Company DUNS437384304
Company NameESAOTE SPA
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 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
GS108056304452634 [Primary]

FDA Product Code

MOSCoil, Magnetic Resonance, Specialty

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-03-05
Device Publish Date2016-09-27

Devices Manufactured by ESAOTE SPA

08056304454287 - PX 1-52023-12-22
08056304454614 - 2CWS-L2023-12-22
08056304454621 - 5CWS-L2023-12-22
08056304454812 - TE 3-82023-12-22
08056304454836 - CX 1-82023-12-22
08056304454935 - LMX 4-202023-12-22
08056304454980 - MyLabX902023-12-22
08056304455000 - LX 3-152023-12-22

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