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MAUDE Adverse Event Report: MICROSURGICAL TECHNOLOGY INC MST; MALYUGIN RING 2.0 6.25
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MICROSURGICAL TECHNOLOGY INC MST; MALYUGIN RING 2.0 6.25
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Model Number
MAL-1001-1
Medical Device Problem Code
Difficult to Fold, Unfold or Collapse (1254)
Health Effect - Clinical Code
Insufficient Information (4580)
Type of Reportable Event
Malfunction
Event or Problem Description
Per surgeon, was bent when ejected and would not function properly.No patient injury.
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Brand Name
MST
Common Device Name
MALYUGIN RING 2.0 6.25
Manufacturer
(Section D)
MICROSURGICAL TECHNOLOGY INC
8415 154th ave ne
redmond WA 98052
Manufacturer
(Section G)
MICROSURGICAL TECHNOLOGY INC
8415 154th ave ne
redmond WA 98052
Manufacturer Contact
yamini nidumolu
8415 154th ave ne
redmond, WA 98052
4255560544
MDR Report Key
24607172
Report Number
3019924-2026-00065
Device Sequence Number
21089115
Product Code
HOC
UDI-Device Identifier
00844685006120
UDI-Public
00844685006120
Combination Product (Y/N)
N
Initial Reporter State
WA
Initial Reporter Country
US
Number of Events Summarized
1
Summary Report (Y/N)
N
Serviced by Third Party (Y/N)
Unknown
Reporter Type
Manufacturer
Report Source
User Facility
Initial Reporter Occupation
Other
Remedial Action
Replace
Type of Report
Initial
Report Date
(Section B)
03/16/2026
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
Operator of Device
Health Professional
Device Model Number
MAL-1001-1
Device Catalogue Number
MAL-1001-1
Device Lot Number
217974
Was Device Available for Evaluation?
No
Type of Report(Section G)
Thirty-Day
Initial Date Received by Manufacturer
02/18/2026
Initial Report FDA Received Date
03/16/2026
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
Unknown
Patient Sequence Number
1
Patient Sex
Unknown
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