HydroTac transp. comf. 6,5x10cm st P10

GUDID 04049500835138

HydroTac transp. comf. 6,5x10cm st P10

PAUL HARTMANN AG

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

• Primary Device ID: 04049500835138
• NIH Device Record Key: 49ef12ec-7d00-4bdb-aaac-b44b00ebda11
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HydroTac transp. comf. 6,5x10cm st P10
• Version Model Number: 6859236
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	04049500835121 [Primary]
GS1	04049500835138 [Package]; Contains: 04049500835121; Package: [10 Units]; In Commercial Distribution
GS1	04049500835145 [Package]; Package: [8 Units]; In Commercial Distribution

FDA Product Code

• NAD: Dressing, Wound, Occlusive

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

On-Brand Devices [HydroTac transp. comf. 6,5x10cm st P10]

• 04052199273709: HydroTac transp. comf. 6,5x10cm st P10
• 04049500835138: HydroTac transp. comf. 6,5x10cm st P10