Symmetry HEANEY 52-5300-H

GUDID 00887482077931

HYST FCP STR DBL TOOTH 9 1/2"

SYMMETRY SURGICAL INC.

Dissection forceps Dissection forceps

• Primary Device ID: 00887482077931
• NIH Device Record Key: abd8c188-4ad9-43fc-a774-8e88829d1449
• Commercial Distribution Discontinuation: 9999-01-01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Symmetry HEANEY
• Version Model Number: 52-5300-H
• Catalog Number: 52-5300-H
• 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	00887482077931 [Primary]

FDA Product Code

• HCZ: Forceps, Surgical, Gynecological

Sterilization

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

[00887482077931]

Moist Heat or Steam Sterilization

[00887482077931]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-06-09

On-Brand Devices [Symmetry HEANEY ]

• 00887482083642: Subclavian Clamp 8"
• 00887482077931: HYST FCP STR DBL TOOTH 9 1/2"
• 00887482004548: Hysterectomy Forceps Heavy Jaws, Double Tooth
• 00887482004531: Hysterectomy Forceps Heavy Single
• 00887482004524: Hysterectomy Forceps LT Single