HF

GUDID 06971519616614

Anji Hengfeng Sanitary Material Co., Ltd

Pressure bandage, non-latex, single-use

• Primary Device ID: 06971519616614
• NIH Device Record Key: 19dbdd11-4304-41be-a07c-d23addfd5524
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HF
• Version Model Number: HFCG02
• Company DUNS: 529497551
• Company Name: Anji Hengfeng Sanitary Material 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: 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	06971519616614 [Primary]

FDA Product Code

• FQM: Bandage, Elastic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-01-12
• Device Publish Date: 2023-01-04

On-Brand Devices [HF]

• 06971519616782: HFFAB1-6
• 06971519616645: HFFAB1-5
• 06971519616614: HFCG02
• 06971519616591: HFFAB1-3
• 06971519616584: HFFAB1-2
• 06971519616577: HFFAB1-1
• 06971519614030: HFFAB1-7