Orthinox 6364-2-230

GUDID 04546540273383

V40 Femoral head

Howmedica Osteonics Corp.

Metallic femoral head prosthesis

• Primary Device ID: 04546540273383
• NIH Device Record Key: 226e9c28-9f13-427f-a238-a5c5559b7e5e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Orthinox
• Version Model Number: 6364-2-230
• Catalog Number: 6364-2-230
• Company DUNS: 058311945
• Company Name: Howmedica Osteonics Corp.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Outer Diameter: 30 Millimeter
• Outer Diameter: 30 Millimeter
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 30 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540273383 [Primary]

FDA Product Code

• JDI: Prosthesis, hip, semi-constrained, metal/polymer, cemented

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-04-06
• Device Publish Date: 2015-09-24

On-Brand Devices [Orthinox]

• 07613153122012: V40 Femoral head
• 07613153122005: V40 Femoral head
• 07613153121992: V40 Femoral head
• 04546540402189: V40 FEM HEAD
• 04546540402172: V40 FEM HEAD
• 04546540402165: V40 FEM HEAD
• 04546540402158: V40 FEM HEAD
• 04546540273390: V40 FEM HEAD
• 04546540273383: V40 Femoral head
• 04546540273369: V40 FEM HEAD
• 04546540273345: V40 FEM HEAD
• 04546540273338: V40 Femoral head
• 04546540273321: V40 FEM HEAD
• 04546540273314: V40 FEM HEAD
• 04546540273307: V40 FEM HEAD
• 04546540273291: V40 FEM HEAD
• 04546540273284: V40 Femoral head
• 04546540273277: V40 FEM HEAD
• 04546540273260: V40 FEM HEAD
• 04546540273376: V40 FEM HEAD