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Dynex

FDA UDI

Class II (US FDA UDI)

by Vilex, Inc.

Identity

Trade Name
Dynex FDA UDI
Generic Name
External orthopaedic fixation system, single-use FDA UDI
Device Name
Drill 2.0x185mm Solid FDA UDI
Model / Reference
DS-Z402-185-20 FDA UDI
Description
Drill 2.0x185mm Solid FDA UDI

Identifiers

Primary DI / UDI-DI
00841731124524 FDA UDI
FDA Product Code
KTT FDA UDI
HTW FDA UDI
GMDN Term
External orthopaedic fixation system, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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: External orthopaedic fixation system, single-use

Dynex by Vilex, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External orthopaedic fixation system, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vilex, Inc.

Sources (1)

  • FDA UDI 562e0bfc-73c6-4e39-b44a-ed2d8cb504b2 33 fields · synced May 29, 2026