Symmetry HOEN 53-1225

GUDID 00887482022122

IVD RONGEUR 6X12

SYMMETRY SURGICAL INC.

Spinal rongeur

• Primary Device ID: 00887482022122
• NIH Device Record Key: 71bf7270-d240-4ca4-b505-c5419b1046c5
• Commercial Distribution Discontinuation: 9999-01-01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Symmetry HOEN
• Version Model Number: 53-1225
• Catalog Number: 53-1225
• Company DUNS: 079641356
• Company Name: SYMMETRY SURGICAL INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00887482022122 [Primary]

FDA Product Code

• HAE: Rongeur, Manual

Sterilization

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

[00887482022122]

Moist Heat or Steam Sterilization

[00887482022122]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-07-12
• Device Publish Date: 2016-05-16

On-Brand Devices [Symmetry HOEN]

• 00887482099353: Retractor Blade
• 00887482099339: Retractor Blades
• 00887482022122: IVD RONGEUR 6X12
• 00887482022115: IVD RONGEUR