Reverse Curette, 7mm 00-9986-010-15;430006

GUDID 00847538001211

Reverse Curette, 7mm

SYMMETRY MEDICAL INC.

Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable

• Primary Device ID: 00847538001211
• NIH Device Record Key: 70c0c975-207f-44a4-99b4-388b9c8aa789
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reverse Curette, 7mm
• Version Model Number: 10-006-000
• Catalog Number: 00-9986-010-15;430006
• Company DUNS: 079881212
• Company Name: SYMMETRY MEDICAL 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: 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	00847538001211 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00847538001211]

Moist Heat or Steam Sterilization

[00847538001211]

Moist Heat or Steam Sterilization

[00847538001211]

Moist Heat or Steam Sterilization

[00847538001211]

Moist Heat or Steam Sterilization

[00847538001211]

Moist Heat or Steam Sterilization

[00847538001211]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-05-20
• Device Publish Date: 2022-05-12

On-Brand Devices [Reverse Curette, 7mm]

• 00847538006339: Reverse Curette, 7mm
• 00847538001211: Reverse Curette, 7mm