VenoTrain business

GUDID 04046445707438

Bauerfeind AG

Compression/pressure sock/stocking, single-use

• Primary Device ID: 04046445707438
• NIH Device Record Key: b05cd21b-e8fb-410f-80f1-21a7165c9b5e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VenoTrain business
• Version Model Number: 20881011700224
• Company DUNS: 315914853
• Company Name: Bauerfeind AG
• Device Count: 1
• 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: true
• 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	04046445707438 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K860826

FDA Product Code

• DWL: Stocking, medical support (to prevent pooling of blood in legs)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-10-07
• Device Publish Date: 2016-09-28

On-Brand Devices [VenoTrain business]

• 04046445899348: 20880011500009
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• 04046445899294: 20880021500009
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• 04046445899195: 20880421700009
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• 04046445708473: 20881022300324
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• 04046445708411: 20881022300232
• 04046445708398: 20881022300224
• 04046445708381: 20881022300223
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• 04046445708060: 20881021600223
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• 04046445708039: 20881021500334
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• 04046445707995: 20881021500324
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• 04046445707919: 20881021500224
• 04046445707902: 20881021500223
• 04046445707896: 20881021500222