BR-120T

GUDID 04540217060962

SHIMADZU CORPORATION

X-ray system tube support, floor stand X-ray system tube support, floor standing X-ray system tube support, floor standing X-ray system tube support, floor standing X-ray system tube support, floor standing X-ray system tube support, floor standing X-ray system tube support, floor standing X-ray system tube support, floor standing
Primary Device ID04540217060962
NIH Device Record Key8656b35f-b9d8-4c5b-b73f-e3f2a7ab46e6
Commercial Distribution StatusIn Commercial Distribution
Brand NameBR-120T
Version Model Number566-16600-85
Company DUNS690558747
Company NameSHIMADZU CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104540217060962 [Primary]

FDA Product Code

IXYHolder, Radiographic Cassette, Wall-Mounted

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-05-06
Device Publish Date2019-04-26

On-Brand Devices [BR-120T]

04540217052790566-16600-65
04540217052783566-16600-64
04540217052776566-16600-05
04540217052769566-16600-04
04540217047901566-16610-93
04540217047895566-16610-92
04540217047864566-16610-83
04540217047857566-16610-82
04540217039517503-67400-53
04540217039487503-67400-36
04540217039456503-67400-33
04540217039425503-67400-30
04540217039395503-67400-27
04540217039357503-67400-23
04540217060962566-16600-85
04540217062683566-16600-86
04540217062478566-16600-50
04540217064779566-16610-86
04540217066810566-16610-87

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