SSCOR/board

GUDID B24523001PLC1

Onboard Suction Device

SSCOR, INC.

Emergency airway clearance suction system, electric
Primary Device IDB24523001PLC1
NIH Device Record Keye0a5a1f2-a3c6-4cd0-aeb0-013be4ae1025
Commercial Distribution StatusIn Commercial Distribution
Brand NameSSCOR/board
Version Model Number23001-PLC
Company DUNS131254971
Company NameSSCOR, INC.
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB24523001PLC1 [Primary]

FDA Product Code

GCXApparatus, Suction, Operating-Room, Wall Vacuum Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-08-23
Device Publish Date2016-09-16

On-Brand Devices [SSCOR/board]

B245250001Onboard Suction Device
B24523001WCKK1Onboard Suction Device
B24523001WCK15Onboard Suction Device
B24523001WC1Onboard Suction Device
B24523001PLC1Onboard Suction Device
B24523001B1Onboard Suction Device
B245230011Onboard Suction Device
B245225001Onboard Suction Device
B24522020LDR12Onboard Suction Device
B24522000RRC15Onboard Suction Device
B24522000PLC1Onboard Suction Device
B24522000GIFA1Onboard Suction Device
B24522000BRAUN1Onboard Suction Device
B245220001Onboard Suction Device

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