Bestex

GUDID 16921340852122

Qingdao Bestex Rubber & Plastic Products Co., Ltd.

Face splash shield, single-use

• Primary Device ID: 16921340852122
• NIH Device Record Key: 2d801668-ad2e-4827-9354-68fe96bcbbd8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bestex
• Version Model Number: FS-3222
• Company DUNS: 530328087
• Company Name: Qingdao Bestex Rubber & Plastic Products 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: false
• Donation Id Number: false
• 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	16921340852122 [Primary]

FDA Product Code

• LYU: Accessory, Surgical Apparel

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: 2022-10-03
• Device Publish Date: 2022-09-23

On-Brand Devices [Bestex]

• 16921340852122: FS-3222
• 06921340851111: FS-3222