AOSHANG

GUDID 06973532970384

Tianjin Aoshang Outdoor Equipment Co.,Ltd

Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use

• Primary Device ID: 06973532970384
• NIH Device Record Key: 49b140dd-2ecc-49f3-b1c1-84441b00dfd6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AOSHANG
• Version Model Number: earloop
• Company DUNS: 554530356
• Company Name: Tianjin Aoshang Outdoor Equipment Co.,Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: 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	06973532970384 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K210030

FDA Product Code

• FXX: Mask, Surgical

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: 2021-08-25
• Device Publish Date: 2021-08-17

On-Brand Devices [AOSHANG]

• 06973532970018: earloop
• 06973532970360: earloop
• 06973532970216: earloop
• 06973532970377: earloop
• 06973532970049: earloop
• 06973532970384: earloop