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Simple Locking Intramedullary (slim) System

FDA UDI

Class I (US FDA UDI)

by Orthopediatrics Canada ULC

Identity

Trade Name
SIMPLE LOCKING INTRAMEDULLARY (SLIM) SYSTEM FDA UDI
Generic Name
Orthopaedic guidewire, single-use FDA UDI
Device Name
BULLET GUIDEWIRE Ø1.1mm - PACKAGE OF 6 FDA UDI
Model / Reference
BLT-GWR100-PKG6 FDA UDI
Description
BULLET GUIDEWIRE Ø1.1mm - PACKAGE OF 6 FDA UDI

Identifiers

Catalog Number
BLT-GWR100-PKG6 FDA UDI
Primary DI / UDI-DI
07540194011923 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 1.1 Millimeter FDA UDI

Category: Orthopaedic guidewire, single-use

Simple Locking Intramedullary (slim) System by Orthopediatrics Canada ULC — 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

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Manufacturer

Sources (1)

  • FDA UDI 46550fef-a00e-4f8b-a7ea-b367cd1e34ff 36 fields · synced May 31, 2026