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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: UNIMAX MEDICAL SYSTEMS INC.; DETACHABLE ENDO POCKET

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UNIMAX MEDICAL SYSTEMS INC.; DETACHABLE ENDO POCKET Back to Search Results
Catalog Number SB979
Medical Device Problem Code Break (1069)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 05/14/2026
Type of Reportable Event Malfunction
Event or Problem Description
The string broke when trying to remove specimen.
 
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Common Device Name
DETACHABLE ENDO POCKET
Manufacturer (Section D)
UNIMAX MEDICAL SYSTEMS INC.
8f-2, no.127, lane 235,
pao chiao rd, xindian dist.
new taipei city, taiwan TW 23 1
TW  TW 231
Manufacturer (Section G)
UNIMAX MEDICAL SYSTEMS INC.
8f-2, no.127, lane 235,
pao chiao road, xindian dist.
new taipei city, 231
TW   231
Manufacturer Contact
kris hsieh
8f-2, no.127, lane 235,
pao chiao road, xindian dist.
new taipei city, 231
TW   231
MDR Report Key25572664
Report Number3007791595-2026-00005
Device Sequence Number5154780
Product Code GCJ
UDI-Device Identifier04714127860909
UDI-Public(01)04714127860909(17)300905(10)6252509154
Combination Product (Y/N)N
Initial Reporter CountryUS
PMA/510(K) Number
K103510
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Distributor
Initial Reporter Occupation Other
Type of Report Initial
Report Date (Section B) 06/22/2026
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Catalogue NumberSB979
Device Lot Number6252509154
Was Device Available for Evaluation? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer Not provided
Initial Report FDA Received Date06/21/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Is the Device Labeled for Single Use? (Y/N) Yes
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Initial
Patient Sequence Number1
Patient SexUnknown
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