← Back to catalogue

Guide Wire Pusher

FDA UDI

Class I (US FDA UDI)

by Orthopedic Designs North America, Inc.

Identity

Trade Name
Guide Wire Pusher FDA UDI
Generic Name
Orthopaedic counter-torque/rod-pushing instrument FDA UDI
Device Name
Guide Wire Pusher FDA UDI
Model / Reference
SLNT40 FDA UDI
Description
Guide Wire Pusher FDA UDI

Identifiers

Catalog Number
SLN-T40 FDA UDI
Primary DI / UDI-DI
B058SLNT401 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic counter-torque/rod-pushing instrument 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic counter-torque/rod-pushing instrument

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

Similar devices

Also classified as Orthopaedic counter-torque/rod-pushing instrument.

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

Manufacturer
Orthopedic Designs North America, Inc.

Sources (1)

  • FDA UDI 29f36471-97d6-40ed-8169-500cd40bdca3 35 fields · synced Jun 1, 2026