Peha-Haft Latex Free 8cm x 4m P1 C140

GUDID 04052199280189

Peha-Haft Latex Free 8cm x 4m P1 C140

PAUL HARTMANN AG

Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Non-adhesive device retention bandage Non-adhesive device retention bandage Non-adhesive device retention bandage Non-adhesive device retention bandage Non-adhesive device retention bandage Non-adhesive device retention bandage Non-adhesive device retention bandage Non-adhesive device retention bandage Non-adhesive device retention bandage Non-adhesive device retention bandage Non-adhesive device retention bandage Non-adhesive device retention bandage Non-adhesive device retention bandage Non-adhesive device retention bandage Non-adhesive device retention bandage Non-adhesive device retention bandage

• Primary Device ID: 04052199280189
• NIH Device Record Key: 4d34c141-4fc7-4b29-8284-a0f7112e23cf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Peha-Haft Latex Free 8cm x 4m P1 C140
• Version Model Number: 9324435
• Company DUNS: 315768788
• Company Name: PAUL HARTMANN AG
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04049500749961 [Primary]
GS1	04052199280189 [Package]; Contains: 04049500749961; Package: [140 Units]; In Commercial Distribution

FDA Product Code

• KGX: Tape And Bandage, Adhesive

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: 2020-09-09
• Device Publish Date: 2020-09-01

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