← Back to catalogue

Atlas™ Humeral Nail System

FDA UDI

Class II (US FDA UDI)

by Orthopedic Designs North America, Inc.

Identity

Trade Name
Atlas™ Humeral Nail System FDA UDI
Generic Name
Humerus intramedullary nail FDA UDI
Device Name
Atlas Humeral Nail System - Nail Ø8mm | 240mm | Right FDA UDI
Model / Reference
AHN08240R FDA UDI
Description
Atlas Humeral Nail System - Nail Ø8mm | 240mm | Right FDA UDI

Identifiers

Catalog Number
AHN-08-240R FDA UDI
Primary DI / UDI-DI
B058AHN08240R1 FDA UDI
510(k) Number
K241484 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Humerus intramedullary nail 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

Yes

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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 240 Millimeter FDA UDI
Outer Diameter — 8 Millimeter FDA UDI

Category: Humerus intramedullary nail

Atlas™ Humeral Nail System by Orthopedic Designs North America, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Humerus intramedullary nail.

Cleared under the same submission

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

Sources (1)

  • FDA UDI 0fb69b77-16e2-4b97-bf97-f0c6b1a9c804 37 fields · synced Jun 8, 2026