Grass

GUDID 00382830017275

Genuine GRASS Platinum Subdermal Needle Electrodes-Reusable

NATUS MANUFACTURING LIMITED

Electromyographic needle electrode, single-use

• Primary Device ID: 00382830017275
• NIH Device Record Key: 2f224e28-dcb5-4355-9453-12ff5f42c4f9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Grass
• Version Model Number: F-E2-72
• Company DUNS: 896421240
• Company Name: NATUS MANUFACTURING LIMITED
• 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	00382830017275 [Primary]

FDA Product Code

• GXY: Electrode, Cutaneous

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-06-11
• Device Publish Date: 2016-08-25

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• 00382830043625: F Series. Subdermal Needle. Molded Safelead
• 00382830043618: F Series. Subdermal Needle. Molded Safelead
• 00382830043601: F Series. Subdermal Needle. Molded Safelead
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