Meicen

GUDID 06977071938102

Guangdong Meicen Medical Equipment Co., Ltd.

Central vacuum pump Central vacuum pump Central vacuum pump Central vacuum pump Central vacuum pump Central vacuum pump Central vacuum pump Central vacuum pump Central vacuum pump Central vacuum pump Central vacuum pump Central vacuum pump Central vacuum pump Central vacuum pump Central vacuum pump Central vacuum pump Central vacuum pump

• Primary Device ID: 06977071938102
• NIH Device Record Key: 81affd01-a9ba-4ead-9898-709045be8e7b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Meicen
• Version Model Number: /
• Company DUNS: 724689169
• Company Name: Guangdong Meicen Medical Equipment Co., Ltd.
• 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: true
• Donation Id Number: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06977071938102 [Primary]

FDA Product Code

• IOQ: Bed, Flotation Therapy, Powered

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: 2024-07-01
• Device Publish Date: 2024-06-21

On-Brand Devices [Meicen]

• 06977071938102: /
• 06977071938003: /
• 06977071937518: /
• 06977071937501: /
• 06977071936009: /
• 06977071930908: /
• 06977071930069: /
• 06977071930014: /