Embody Cannula EM-A001-01

GUDID 00810063820169

Embody Cannula, 40mm

Embody, Inc.

Arthroscopic access cannula, single-use

• Primary Device ID: 00810063820169
• NIH Device Record Key: f28d773a-d0f3-40d4-a795-035a7fc190f2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Embody Cannula
• Version Model Number: EM-A001-01
• Catalog Number: EM-A001-01
• Company DUNS: 079544913
• Company Name: Embody, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• 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: 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
GS1	00810063820169 [Primary]

FDA Product Code

• GEA: Cannula, Surgical, General & Plastic Surgery

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-06-10
• Device Publish Date: 2022-06-02

On-Brand Devices [Embody Cannula]

• 00810063820183: Embody Cannula, 80mm
• 00810063820176: Embody Cannula, 60mm
• 00810063820169: Embody Cannula, 40mm