Right Way Medical

GUDID 26972620112358

BQ PLUS MEDICAL CO., LTD.

Basic intravenous administration set, noninvasive
Primary Device ID26972620112358
NIH Device Record Key8f861800-6da7-4fe5-9bef-8ddd16581fa7
Commercial Distribution StatusIn Commercial Distribution
Brand NameRight Way Medical
Version Model NumberRWM-IFRF01
Company DUNS544463583
Company NameBQ PLUS MEDICAL CO., LTD.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS126972620112358 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FPASet, Administration, Intravascular

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[26972620112358]

Ethylene Oxide


[26972620112358]

Ethylene Oxide


[26972620112358]

Ethylene Oxide


[26972620112358]

Ethylene Oxide


[26972620112358]

Ethylene Oxide


[26972620112358]

Ethylene Oxide


[26972620112358]

Ethylene Oxide


[26972620112358]

Ethylene Oxide


[26972620112358]

Ethylene Oxide


[26972620112358]

Ethylene Oxide


[26972620112358]

Ethylene Oxide


[26972620112358]

Ethylene Oxide


[26972620112358]

Ethylene Oxide


[26972620112358]

Ethylene Oxide


[26972620112358]

Ethylene Oxide


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-03-31
Device Publish Date2025-03-21

On-Brand Devices [Right Way Medical]

26972620112358RWM-IFRF01
16972620112351RWM-IFRF01
06972620112347RWM-IFRF01

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