← Back to catalogue

Ball Tip Wire

FDA UDI

Class I (US FDA UDI)

by Orthopedic Designs North America, Inc.

Identity

Trade Name
Ball Tip Wire FDA UDI
Generic Name
Orthopaedic guidewire, single-use FDA UDI
Device Name
Ball Tip Wire, 3mm x 900mm FDA UDI
Model / Reference
THNT34 FDA UDI
Description
Ball Tip Wire, 3mm x 900mm FDA UDI

Identifiers

Catalog Number
THN-T34 FDA UDI
Primary DI / UDI-DI
B058THNT341 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic guidewire, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 3 Millimeter FDA UDI
Length — 900 Millimeter FDA UDI

Category: Orthopaedic guidewire, single-use

Ball Tip Wire by Orthopedic Designs North America, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic guidewire, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 486ee7af-1a45-43a4-9bb3-02ce3307d845 36 fields · synced Jun 8, 2026