Hemorrhoid Ligator AL8000

GUDID 00850348007342

Adler Hemorrhoid Ligator

ADLER MICROMED, INC.

Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator Haemorrhoid ligator

• Primary Device ID: 00850348007342
• NIH Device Record Key: 13d12800-738e-45cf-948e-17e9a3e86817
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hemorrhoid Ligator
• Version Model Number: AL8000
• Catalog Number: AL8000
• Company DUNS: 080298464
• Company Name: ADLER MICROMED, 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850348007335 [Primary]
GS1	00850348007342 [Package]; Contains: 00850348007335; Package: [25 Units]; In Commercial Distribution

FDA Product Code

• FHN: Ligator, Hemorrhoidal

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-10-09
• Device Publish Date: 2019-10-01

Devices Manufactured by ADLER MICROMED, INC.

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• 00850348007342 - Hemorrhoid Ligator: 2019-10-09Adler Hemorrhoid Ligator
• 00850348007342 - Hemorrhoid Ligator: 2019-10-09 Adler Hemorrhoid Ligator