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Mermaid Medical® Guidewire

FDA UDI

Class II (US FDA UDI)

by Techdevice Corporation

Identity

Trade Name
Mermaid Medical® Guidewire FDA UDI
Generic Name
Peripheral vascular guidewire, manual FDA UDI
Device Name
Mermaid Medical® Guidewire .035” x 150 cm, 7.5 cm (Straight Tip) FDA UDI
Model / Reference
G60135150 FDA UDI
Description
Mermaid Medical® Guidewire .035” x 150 cm, 7.5 cm (Straight Tip) FDA UDI

Identifiers

Catalog Number
G60135150 FDA UDI
Primary DI / UDI-DI
00850758007031 FDA UDI
510(k) Number
K053251 FDA UDI
FDA Product Code
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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 0.035 Inch FDA UDI
Length — 150 Centimeter FDA UDI

Category: Peripheral vascular guidewire, manual

Mermaid Medical® Guidewire by Techdevice Corporation — 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

K053251 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Techdevice Corporation

Sources (1)

  • FDA UDI 9a83a76e-77db-4fc6-9f5d-a9dab7d2775a 36 fields · synced Jun 6, 2026