KV-6 Suction Pump K10026147

GUDID 07612367044974

Suction Pump 071.0005-03

Medela AG

General-purpose suction system, line-powered

• Primary Device ID: 07612367044974
• NIH Device Record Key: 3b0d38b6-9c89-4f9b-b589-24c83e218af4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KV-6 Suction Pump
• Version Model Number: 200.5625
• Catalog Number: K10026147
• Company DUNS: 488293218
• Company Name: Medela AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07612367044974 [Primary]
GS1	07612367052467 [Direct Marking]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150134

FDA Product Code

• BTA: Pump, Portable, Aspiration (Manual Or Powered)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-10-03

On-Brand Devices [KV-6 Suction Pump]

• 07612367052467: Suction Pump 071.0005-04
• 07612367044974: Suction Pump 071.0005-03