Orthinox 6364-2-032

GUDID 04546540273291

V40 FEM HEAD

Howmedica Osteonics Corp.

Metallic femoral head prosthesis Metallic femoral head prosthesis Metallic femoral head prosthesis Metallic femoral head prosthesis Metallic femoral head prosthesis Metallic femoral head prosthesis Metallic femoral head prosthesis Metallic femoral head prosthesis Metallic femoral head prosthesis Metallic femoral head prosthesis Metallic femoral head prosthesis Metallic femoral head prosthesis Metallic femoral head prosthesis Metallic femoral head prosthesis Metallic femoral head prosthesis

• Primary Device ID: 04546540273291
• NIH Device Record Key: fcd50cb7-2907-4ddf-a6bc-2a535a88a6c9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Orthinox
• Version Model Number: 6364-2-032
• Catalog Number: 6364-2-032
• 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: 32 Millimeter
• Outer Diameter: 32 Millimeter
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540273291 [Primary]

FDA Product Code

• LWJ: Prosthesis, hip, semi-constrained, metal/polymer, uncemented

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