MOLLI

GUDID 00850024195165

MOLLI re.markable (w/ 12cm Introducer) Single Unit

Molli Surgical Inc

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• Primary Device ID: 00850024195165
• NIH Device Record Key: 677217cd-e98b-402f-a466-fd0da88ccde7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MOLLI
• Version Model Number: RM0112
• Company DUNS: 204044952
• Company Name: Molli Surgical Inc
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• 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: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850024195165 [Primary]

FDA Product Code

• KDC: Instrument, Surgical, Disposable

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-04-07
• Device Publish Date: 2023-03-30

On-Brand Devices [MOLLI]

• 00850024195035: MOLLI Introducer & MOLLI Marker (8 cm, 14GA) For use with the MOLLI System Note, the Introducer
• 00850024195011: MOLLI Tablet
• 00850024195004: MOLLI Wand
• 00850024195080: MOLLI Introducer and MOLLI Marker (12 cm, 14GA) For use with the MOLLI System Note, the Introduc
• 00850024195165: MOLLI re.markable (w/ 12cm Introducer) Single Unit
• 00850024195158: MOLLI 2 Tablet
• 00850024195141: MOLLI 2 Wand
• 00850024195172: MOLLI Pole Clamp
• 00850024195219: MOLLI OncoPen