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Simple Locking Intramedullary (slim) System

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref SLM-20-300Model SLIM ROD

by Orthopediatrics Canada ULC

Identity

Trade Name
The Simple Locking Intra Medullary System EUDAMED
SIMPLE LOCKING INTRAMEDULLARY (SLIM) SYSTEM FDA UDI
Generic Name
Arthrodesis intramedullary nail, non-distracting FDA UDI
Device Name
SLIM Rod Ø2.0mm x 300mm FDA UDI
Model / Reference
SLM-20-300 EUDAMEDFDA UDI
SLIM ROD EUDAMED
Description
SLIM Rod Ø2.0mm x 300mm FDA UDI

Identifiers

Catalog Number
SLM-20-300 FDA UDI
Primary DI / UDI-DI
07540194002778 EUDAMEDFDA UDI
Basic UDI-DI
7540194SLM-NAILSFD EUDAMED
510(k) Number
K143355 FDA UDI
FDA Product Code
HSB FDA UDI
EMDN Code
P09120201 INTRAMEDULLARY NAILS EUDAMED
GMDN Term
Arthrodesis intramedullary nail, non-distracting FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Market of Registration
Sweden EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Sutures

Yes

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

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

Dimensions & Sizes

Size
Outer Diameter — 2 Millimeter FDA UDI
Length — 300 Millimeter FDA UDI

Category: Arthrodesis intramedullary nail, non-distracting

Simple Locking Intramedullary (slim) System by Orthopediatrics Canada ULC — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

Also classified as Arthrodesis intramedullary nail, non-distracting.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 41820cf8-83d6-4bf6-b964-7e2277fa7c51 38 fields · synced Jun 14, 2026
  • EUDAMED 1548a321-0cc9-4f89-9bbf-5a461ca6a6b8 61 fields · synced Jun 11, 2026