BREATHING BAG 2107102

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2004-02-20 for BREATHING BAG 2107102 manufactured by Rusch U.k. Ltd.

Event Text Entries

[337891] Customer reports bag split during use.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8010092-2004-00017
MDR Report Key528004
Report Source05
Date Received2004-02-20
Date of Report2004-02-19
Date Mfgr Received2004-02-18
Date Added to Maude2004-06-04
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactROLANDA SCOTT, COORDINATOR
Manufacturer Street2450 MEADOWBROOK PKWY
Manufacturer CityDULUTH GA 30136
Manufacturer CountryUS
Manufacturer Postal30136
Manufacturer Phone7706230816
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBREATHING BAG
Generic NameANESTHESIA
Product CodeBYW
Date Received2004-02-20
Model NumberNA
Catalog Number2107102
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key517193
ManufacturerRUSCH U.K. LTD
Manufacturer AddressPORTADOWN RD. NORTHERN IRELAND UK BT66 8RD
Baseline Brand NameLATEX BREATHING BAG
Baseline Generic NameLATEX BREATHING BAG
Baseline Model NoNA
Baseline Catalog No2107102
Baseline IDNA
Baseline Device FamilyBREATHING BAG
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentY
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
10 2004-02-20

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