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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
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
FULL 6.0mm BULLET CADDY FDA UDI
Model / Reference
BLT-CFL-60 FDA UDI
Description
FULL 6.0mm BULLET CADDY FDA UDI

Identifiers

Catalog Number
BLT-CFL-60 FDA UDI
Primary DI / UDI-DI
07540194012210 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) 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

Yes

FDA UDI

Implantable

Yes

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

No

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: Orthopaedic bone screw (non-sliding)

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 Orthopaedic bone screw (non-sliding).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 530eb8e2-c856-4849-b4fd-7e9500ee392f 35 fields · synced Jun 8, 2026