NBAC 1.5T SMS, Flex

GUDID 04260486610230

No description.

LMT Medical Systems GmbH

MRI system coil, radio-frequency
Primary Device ID04260486610230
NIH Device Record Key88505686-24ec-4795-af1b-4679d5294c2e
Commercial Distribution StatusIn Commercial Distribution
Brand NameNBAC 1.5T SMS, Flex
Version Model Number0800150
Company DUNS312688686
Company NameLMT Medical Systems GmbH
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
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 Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+49451580980
Emailinfo@lmt-medicalsystems.com
Phone+49451580980
Emailinfo@lmt-medicalsystems.com
Phone+49451580980
Emailinfo@lmt-medicalsystems.com
Phone+49451580980
Emailinfo@lmt-medicalsystems.com
Phone+49451580980
Emailinfo@lmt-medicalsystems.com
Phone+49451580980
Emailinfo@lmt-medicalsystems.com
Phone+49451580980
Emailinfo@lmt-medicalsystems.com
Phone+49451580980
Emailinfo@lmt-medicalsystems.com
Phone+49451580980
Emailinfo@lmt-medicalsystems.com
Phone+49451580980
Emailinfo@lmt-medicalsystems.com
Phone+49451580980
Emailinfo@lmt-medicalsystems.com
Phone+49451580980
Emailinfo@lmt-medicalsystems.com
Phone+49451580980
Emailinfo@lmt-medicalsystems.com
Phone+49451580980
Emailinfo@lmt-medicalsystems.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104260486610230 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MOSCoil, Magnetic Resonance, Specialty

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-08-31
Device Publish Date2020-08-23

On-Brand Devices [NBAC 1.5T SMS, Flex]

04260486610230No description.
04260486610940No description.

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