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Parallel Wire Guide, for φ2.5 Guide Wire, Adjustable

FDA UDI

Class II (US FDA UDI)

by Double Medical Technology Inc.

Identity

Trade Name
Parallel Wire Guide, for φ2.5 Guide Wire, Adjustable FDA UDI
Generic Name
Orthopaedic guidewire, reusable FDA UDI
Model / Reference
110200600 FDA UDI

Identifiers

Catalog Number
110200600 FDA UDI
Primary DI / UDI-DI
06902139111258 FDA UDI
510(k) Number
K130108 FDA UDI
FDA Product Code
HWC FDA UDI
HRS FDA UDI
GMDN Term
Orthopaedic guidewire, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic guidewire, reusable

Parallel Wire Guide, for φ2.5 Guide Wire, Adjustable by Double Medical Technology Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic guidewire, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 32760f6e-5137-4da6-b029-64506e42ad60 35 fields · synced May 30, 2026