BAROVAC® Evacuator Closed Wound Drainage System(PP)

GUDID 08806369427616

BAROVAC PP 400-3.2

Sewoon Medical Co., Ltd.

Closed-wound drainage kit

• Primary Device ID: 08806369427616
• NIH Device Record Key: 47859137-5eb6-4c33-aa75-92bf9fc69b2c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BAROVAC® Evacuator Closed Wound Drainage System(PP)
• Version Model Number: PP400M(3.2)N273
• Company DUNS: 687784405
• Company Name: Sewoon Medical Co., Ltd.
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08806369427616 [Primary]

FDA Product Code

• GCY: Apparatus, Suction, Single Patient Use, Portable, Nonpowered

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: 2023-08-04
• Device Publish Date: 2023-07-27

On-Brand Devices [BAROVAC® Evacuator Closed Wound Drainage System(PP)]

• 08806369498722: BAROVAC PP 400-3.2
• 08806369498708: BAROVAC PP 200-4.8
• 08806369456500: BAROVAC PP 800-4.8
• 08806369456104: BAROVAC PP 400-4.8
• 08806369456081: BAROVAC PP 400-3.2
• 08806369456043: BAROVAC PP 400-4.8
• 08806369456029: BAROVAC PP 400-3.2
• 08806369455503: BAROVAC PP 200-3.2
• 08806369427777: PP400L(4.8)S
• 08806369427739: PP400M(3.2)S
• 08806369427692: BAROVAC PP 400-2.4
• 08806369427654: PP400L(4.8)N273
• 08806369427616: BAROVAC PP 400-3.2