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Hinge Pediatric Plating System

FDA UDI

Class I (US FDA UDI)

by Orthopediatrics Canada ULC

Identity

Trade Name
HINGE PEDIATRIC PLATING SYSTEM FDA UDI
Generic Name
Orthopaedic guidewire, single-use FDA UDI
Device Name
HINGE PLATE GUIDE WIRE Ø1.1mm -GEN2 - PACK OF 2 FDA UDI
Model / Reference
HP-GWR250-PKG2 FDA UDI
Description
HINGE PLATE GUIDE WIRE Ø1.1mm -GEN2 - PACK OF 2 FDA UDI

Identifiers

Catalog Number
HP-GWR250-PKG2 FDA UDI
Primary DI / UDI-DI
07540194015822 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

Hinge Pediatric Plating 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 f82243b9-35f8-4781-9aef-94b9a9fcce9d 36 fields · synced Jun 8, 2026