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Mirage

FDA UDI

Class II (US FDA UDI)

by Micro Therapeutics, Inc.

Identity

Trade Name
Mirage FDA UDI
Generic Name
Peripheral vascular guidewire, manual FDA UDI
Device Name
GUIDEWIRE 103-0608 V08 MIRAGE FDA UDI
Model / Reference
103-0608 FDA UDI
Description
GUIDEWIRE 103-0608 V08 MIRAGE FDA UDI

Identifiers

Primary DI / UDI-DI
00763000294120 FDA UDI
510(k) Number
K193548 FDA UDI
K201690 FDA UDI
FDA Product Code
MOF FDA UDI
DQX FDA UDI
GMDN Term
Peripheral vascular guidewire, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1330 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Peripheral vascular guidewire, manual

Mirage by Micro Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular guidewire, manual.

Cleared under the same submission

K193548 also covers:

K201690 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Micro Therapeutics, Inc.

Sources (1)

  • FDA UDI 5013899c-4092-464b-b48e-3ec57ba9ea50 36 fields · synced May 31, 2026