customized

GUDID 16921340872113

Qingdao Bestex Rubber & Plastic Products Co., Ltd.

Face splash shield, single-use

• Primary Device ID: 16921340872113
• NIH Device Record Key: 6387b2f2-f38f-493c-bb50-37912e5491b2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: customized
• 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	16921340872113 [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: 2023-06-26
• Device Publish Date: 2023-06-16

On-Brand Devices [customized]

• 16921340885113: XXL
• 16921340884116: XL
• 16921340883119: L
• 16921340882112: M
• 16921340881115: S
• 16921340873110: FS-3224
• 16921340872113: FS-3222
• 16921340871116: FS-3219
• 06921340885116: XXL
• 06921340884119: XL
• 06921340883112: L
• 06921340882115: M
• 06921340881118: S
• 06921340873113: FS-3224
• 06921340872116: FS-3222
• 06921340871119: FS-3219