Meicen

GUDID 06977071937518

Guangdong Meicen Medical Equipment Co., Ltd.

Patient positioning thermoplastic mould material

• Primary Device ID: 06977071937518
• NIH Device Record Key: 3e011dfa-88c7-4d4f-8504-af007932acc2
• 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: true
• 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	06977071937518 [Primary]

FDA Product Code

• EPP: Splint, Nasal

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: /