AECOR 250 Neck Pro

GUDID 00850001456234

Omm Imports Inc.

Hand-held electric massager

• Primary Device ID: 00850001456234
• NIH Device Record Key: db458f79-1554-46e5-a28d-9288f96f4b4f
• Commercial Distribution Discontinuation: 2031-07-01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AECOR 250 Neck Pro
• Version Model Number: AE250
• Company DUNS: 010000704
• Company Name: Omm Imports 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850001456234 [Primary]

FDA Product Code

• ISA: Massager, Therapeutic, Electric

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: 2022-07-04
• Device Publish Date: 2022-06-24

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