← Back to catalogue

Simple Locking Intramedullary (slim) System

FDA UDI

Class II (US FDA UDI)

by Orthopediatrics Canada ULC

Identity

Trade Name
SIMPLE LOCKING INTRAMEDULLARY (SLIM) SYSTEM FDA UDI
Generic Name
General internal orthopaedic fixation system implantation kit FDA UDI
Device Name
FULL PEG IMPLANT & INSTRUMENT CASE RENTAL FDA UDI
Model / Reference
PEG-CSFRENT FDA UDI
Description
FULL PEG IMPLANT & INSTRUMENT CASE RENTAL FDA UDI

Identifiers

Catalog Number
PEG-CSFRENT FDA UDI
Primary DI / UDI-DI
07540194012104 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
General internal orthopaedic fixation system implantation kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 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

Yes

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

Category: General internal orthopaedic fixation system implantation kit

Simple Locking Intramedullary (slim) System by Orthopediatrics Canada ULC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General internal orthopaedic fixation system implantation kit.

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
Orthopediatrics Canada ULC

Sources (1)

  • FDA UDI b35ebde5-a9c3-434c-a0fb-a05820ad8a05 36 fields · synced May 31, 2026