DynaClip Quattro

GUDID M9703000130000

Procedure Pack, Dynaclip Quattro

Medshape, Inc.

Joint prosthesis implantation kit, single-use

• Primary Device ID: M9703000130000
• NIH Device Record Key: fb0aa57f-ad52-46f3-b96b-76e7ef5ab117
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DynaClip Quattro
• Version Model Number: 3000-13-000
• Company DUNS: 601306413
• Company Name: Medshape, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M9703000130000 [Primary]

FDA Product Code

• KDD: Kit, Surgical Instrument, Disposable

Sterilization

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

[M9703000130000]

Radiation Sterilization

[M9703000130000]

Radiation Sterilization

[M9703000130000]

Radiation Sterilization

[M9703000130000]

Radiation Sterilization

[M9703000130000]

Radiation Sterilization

[M9703000130000]

Radiation Sterilization

[M9703000130000]

Radiation Sterilization

[M9703000130000]

Radiation Sterilization

[M9703000130000]

Radiation Sterilization

[M9703000130000]

Radiation Sterilization

[M9703000130000]

Radiation Sterilization

[M9703000130000]

Radiation Sterilization

[M9703000130000]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-08-12
• Device Publish Date: 2023-03-15

On-Brand Devices [DynaClip Quattro]

• M9703000130000: Procedure Pack, Dynaclip Quattro
• M9703000112220200: QUATTRO DYNACLIP STAPLE, 22X20X20