VenoTrain micro

GUDID 04046445193231

Bauerfeind AG

Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use Compression/pressure sock/stocking, single-use

• Primary Device ID: 04046445193231
• NIH Device Record Key: c163e76b-0b40-43e6-9103-c854c5cbc6fb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VenoTrain micro
• Version Model Number: 21810014600223
• 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: true
• Serial Number: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	04046445193231 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-08-03
• Device Publish Date: 2020-07-24

On-Brand Devices [VenoTrain micro]

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