Reliance Fusion Light

GUDID 00841982101701

WLJ1HZ083B, Sterilization Wrap, Reliance Fusion Light, Blue and green bonded alternating sheets, 54 x 72 inches [] 48 applications per case. As used, blue sheet is outer layer.

AHLSTROM NONWOVENS LLC

Sterilization packaging, single-use

• Primary Device ID: 00841982101701
• NIH Device Record Key: 7fe73d39-9101-41a3-ab01-e163b9126b7d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reliance Fusion Light
• Version Model Number: FL05470
• Company DUNS: 039993345
• Company Name: AHLSTROM NONWOVENS LLC
• Device Count: 48
• 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: true
• Manufacturing Date: false
• 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

Customer Support Contacts

• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com
• Phone: 8606548300
• Email: medical@ahlstrom.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841982101701 [Unit of Use]
GS1	00841982101718 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K230137

FDA Product Code

• FRG: Wrap, Sterilization

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: 2024-03-19
• Device Publish Date: 2024-03-11

On-Brand Devices [Reliance Fusion Light]

• 00841982101701: WLJ1HZ083B, Sterilization Wrap, Reliance Fusion Light, Blue and green bonded alternating sheets,
• 00841982101688: WLJ1HZ083B, Sterilization Wrap, Reliance Fusion Light, Blue and green bonded alternating sheets,
• 00841982101664: WLJ1HZ083B, Sterilization Wrap, Reliance Fusion Light, Blue and green bonded alternating sheets,
• 00841982101640: WLJ1HZ083B, Sterilization Wrap, Reliance Fusion Light, Blue and green bonded alternating sheets,
• 00841982101626: WLJ1HZ083B, Sterilization Wrap, Reliance Fusion Light, Blue and green bonded alternating sheets,
• 00841982101602: WLJ1HZ083B, Sterilization Wrap, Reliance Fusion Light, Blue and green bonded alternating sheets,
• 00841982101589: WLJ1HZ083B, Sterilization Wrap, Reliance Fusion Light, Blue and green bonded alternating sheets,
• 00841982101565: WLJ1HZ083B, Sterilization Wrap, Reliance Fusion Light, Blue and green bonded alternating sheets,
• 00841982101541: WLJ1HZ083B, Sterilization Wrap, Reliance Fusion Light, Blue and green bonded alternating sheets,
• 00841982101527: WLJ1HZ083B, Sterilization Wrap, Reliance Fusion Light, Blue and green bonded alternating sheets,