DEVICE: HEADLINER (04987350781031)

Device Identifier (DI) Information

HEADLINER
GM1422
In Commercial Distribution
RG*EA1420SA
TERUMO CORPORATION
04987350781031
GS1

1
690543319 *Terms of Use
HEADLINER Hydrophilic Coated Guidewire
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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. The copyright and database rights in the original GMDN materials are owned by The GMDN Agency Ltd 2005-2023. Used under licence from The GMDN Agency Ltd.

GMDN Term Code GMDN Term Name GMDN Term Definition GMDN Term Status [?] Implantable?
35094 Cardiac/peripheral vascular guidewire, single-use
A long, thin, sterile wire intended to be percutaneously placed into the cardiac vasculature (ventricles or coronary vessels) to function as a guide for the introduction, positioning, and/or operation of a device (e.g., catheter, pacing lead); it may also be used in the peripheral vasculature. It may be made of metal (e.g., stainless steel, Nitinol), or polymer and/or glass materials to provide MRI-compatibility, with or without coating, and is available in a variety of distal tip designs. It is used for various diagnostic and interventional procedures, and may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device.
Active false
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FDA Product Code

[?]
Product Code Product Code Name
DQX WIRE, GUIDE, CATHETER
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
Premarket Submission Number Not Available/Not Released
No CLOSE

Sterilization

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

[?]
Storage and Handling
Special Storage Condition, Specify: FRAGILE. KEEP AWAY FROM RAIN. KEEP AWAY FROM SUNLIGHT. LIMIT STACK TO10.
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Clinically Relevant Size

[?]
Size Type Text
Device Size Text, specify: 45 degree Shapeable type
Outer Diameter: 0.36 Millimeter
Length: 200 Centimeter
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Device Record Status

53738487-fd19-466a-bcf6-eb1f155bf97b
March 29, 2018
2
September 09, 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
54987350781036 5 04987350781031 In Commercial Distribution Carton
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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(714)247-8000
customerservice@microvention.com
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