Suprasorb A 20440

GUDID 05060786981509

SPECIALITY FIBRES AND MATERIALS LIMITED

Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial

• Primary Device ID: 05060786981509
• NIH Device Record Key: 306d9b72-b919-4c3e-b97e-57103031a272
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Suprasorb A
• Version Model Number: Suprasorb A L130 5x5cm
• Catalog Number: 20440
• Company DUNS: 219041423
• Company Name: SPECIALITY FIBRES AND MATERIALS LIMITED
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060786981509 [Primary]

FDA Product Code

• NAC: Dressing, Wound, Hydrophilic

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: 2024-05-30
• Device Publish Date: 2024-05-22

On-Brand Devices [Suprasorb A]

• 05060786981509: Suprasorb A L130 5x5cm
• 05060786981493: Suprasorb A L130 2x30cm
• 05060786981486: Suprasorb A L130 10x20cm
• 05060786981479: Suprasorb A L130 10x12.5cm
• 05060786981462: Suprasorb A L130 10x10cm