DEVICE: FLASH Ostial System (M917OCB5014BA0)

Device Identifier (DI) Information

FLASH Ostial System
OCB5014BA
In Commercial Distribution
OCB5014BA
Verge Medical, Inc.
M917OCB5014BA0
HIBCC

1
078708447 *Terms of Use
FLASH Ostial System, Dual Balloon Angioplasty Catheter, 5.0mm x 12mm
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Device Characteristics

Labeling does not contain MRI Safety Information
No
No
Yes
Yes
No
No
No
No

GMDN

[?]

GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.

GMDN Term Code GMDN Term Name GMDN Term Definition GMDN Term Status [?] Implantable?
47732 Coronary angioplasty balloon catheter, basic
A flexible tube designed for percutaneous transluminal coronary angioplasty (PTCA) to dilate a stenotic coronary artery by controlled inflation of a distensible balloon(s) at its distal tip. It is typically available as: 1) an over-the-wire (OTW) type that has a double or triple-lumen, one for the guidewire and one or two for single- or double-balloon inflation; and 2) a rapid exchange (RX) type with a single-lumen. It is available in various sizes for the dilatation of small, narrowed, or obstructed coronary arteries or bypass grafts. It may also be intended for pre- or post-dilatation of a balloon-expandable stent (not included) in the coronary arteries. This is a single-use device.
Active false
17184 Peripheral angioplasty balloon catheter, basic
A sterile, non-drug-eluting, flexible tube designed for percutaneous transluminal angioplasty (PTA) to dilate a stenotic peripheral (i.e., non-cerebral, non-coronary) artery by controlled inflation of a distensible balloon(s) at its distal tip; it may also be intended for positioning and expansion of a stent/stent-graft. It is available as an over-the-wire (OTW) type with multiple lumens, or a rapid exchange (RX) type with a single lumen. Some types may include cutting/scoring elements (e.g., microsurgical blades, dual wire configurations) to score/modify the plaque. This is a single-use device.
Active false
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FDA Product Code

[?]
Product Code Product Code Name
LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous
DQY Catheter, Percutaneous
LIT Catheter, Angioplasty, Peripheral, Transluminal
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
K113775 000
K120738 000
K122178 000
K122379 000
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Sterilization

Yes
No
Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

[?]
Storage and Handling
Special Storage Condition, Specify: Store in a dry location at room temperature (~23°C)
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Clinically Relevant Size

[?]
Size Type Text
Device Size Text, specify: Distal Balloon Diameter: 5.0mm
Device Size Text, specify: Distal Balloon Length: 12mm
Device Size Text, specify: Catheter Length: 135cm
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Device Record Status

fd00c644-4d65-4e99-bba4-12a03ac5fad6
May 01, 2025
7
September 22, 2016
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Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]
Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
No Package DIs found
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Secondary DI

[?]
Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

[?]
Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
Yes
No
Yes
No
No CLOSE

Customer Contact

[?]
1-844-352-7411
info@ostialcorp.com
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